[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT04349059":3,"trial-entities:NCT04349059":191,"trial-summary:NCT04349059":196},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":20,"study_type":25,"primary_purpose":26,"phases":27,"enrollment_info":29,"interventions":32,"primary_outcomes":42,"secondary_outcomes":47,"sex":58,"minimum_age":59,"maximum_age":60,"healthy_volunteers":61,"eligibility_criteria":62,"std_ages":111,"locations":113,"central_contacts":129,"overall_officials":134,"references":137,"see_also_links":190},"NCT04349059","2019-10465","The Impact of Dietary Pattern on Erectile Function","The Impact of a Plant-Based Diet Versus an Animal-Based Diet on Erectile Function in Healthy Men With Normal Erectile Function: The ERECTION Study","RECRUITING","2026-12","2026-07","2026-07-24","2023-10-30","Montefiore Medical Center","OTHER",false,"The goal of this study is to determine whether erectile function is impacted by dietary patterns in healthy men with normal erectile function.","Visit 1:\n\nAfter reviewing and signing consent, subjects will be screened for the study. Screening will consist of the following:\n\n* Complete International Index of Erectile Function (IIEF) questionnaire.\n* Record medical history, concomitant medications\n* Measure height and weight, calculate BMI\n* Vitals\n* Draw blood for total testosterone, sex hormone binding globulin and Thyroid Stimulating Hormone\n* Query subject regarding the presence of genital rash or lesions. Subjects will be asked, \"do you have a rash or lesion on your penis or surrounding area?\"\n\nIf the IIEF score is abnormal, subjects will be advised to contact their primary care provider.\n\nEach subject will be contacted by phone with their blood results. If abnormal subject will be given the recommendation to contact his primary care provider.\n\nIf an abnormal finding is identified during screening, such as an abnormal STOP-bang score, subject will be given the recommendation to contact his primary care provider.\n\nIf the subject has no primary care provider, contact information for primary care will be given.\n\nSubjects meeting inclusion and exclusion criteria will be randomized into the study, into either Sequence One or Sequence Two. Once enrolled, subjects will be asked to not modify their dietary habits throughout the duration of the study other than during the two evenings and two full days when food is provided (see below).\n\nSequence One:\n\nVisit 2:\n\nSubjects will return to the study center in the morning after having fasted (other than consuming water) since 11pm the night before. They will have been asked to not brush their teeth or use mouthwash and\u002For other breath fresheners that morning. Anthropomorphic and blood pressure and heart rate recordings will be made. Saliva will be stored for NO measurement. Blood will be drawn and stored. Urine will be collected and stored.\n\nSubjects will be taught how to use the Rigiscan™ device. Subjects will receive one plant-based dinner (food will be provided by Montefiore-Einstein Food Services.) Subjects will then leave the study center and they will consume their usual diet until 5pm. For the rest of the evening until 11pm they will consume only the dinner provided. Water will be the only beverage allowed after 5pm. Dinner should be consumed at 8:30pm EST. Subjects will text pictures of everything they consume (eat or drink) after 5pm to Dr. Ostfeld or to a study representative and s\u002Fhe will have text or verbal contact with the subject at least once that evening. That night, subjects will do a Rigiscan™ assessment overnight at their home. The time the subject goes to bed and the time the subject wakes up for the day should be recorded. The subject agrees to be in bed with Rigiscan™ on (other than for emergency or needed trips to the bathroom) for at least seven hours.\n\nVisit 3 Subjects will return to the study center the morning after the Rigiscan™ assessment and bring the Rigiscan™ device with them. They will have been fasting other than drinking water since 11pm the night before. They will have been asked to not brush their teeth or use mouthwash and\u002For other breath fresheners that morning. Anthropomorphic and blood pressure and heart rate recordings will be taken. Saliva will be stored for NO measurement. Blood will be drawn and stored. Urine will be collected and stored.\n\nSubjects will then receive one full day of plant-based meals (food will be provided by Montefiore-Einstein Food Services.) Subjects will be encouraged to eat breakfast at the study center after the initial anthropomorphic measures are made, saliva is obtained, and blood is drawn. Subjects will text pictures of all they consume during that day to Dr. Ostfeld and\u002For to a study representative and s\u002Fhe will have text or verbal contact with the subject at least twice during that day. Dinner should be consumed at 8:30pm, EST. Subjects will fast other than water after 11pm. That night, subjects will do a Rigiscan™ assessment overnight at their home. Black coffee and\u002For tea is permitted only before noon. The time the subject goes to bed and the time the subject wakes up for the day should be recorded. The subject agrees to be in bed with Rigiscan™ on (other than for emergency or needed trips to the bathroom) for at least seven hours.\n\nVisit 4 Subjects will return to the study center the morning after the Rigiscan™ assessment and bring the Rigiscan™ device with them. They will have been asked to not brush their teeth or use mouthwash and\u002For other breath fresheners that morning. Anthropomorphic and blood pressure and heart rate recordings will be taken. Saliva will be stored for NO measurement. Blood will be drawn and stored. Urine will be collected and stored.\n\nThere will then be a washout period for 8-12 days and subjects will be instructed to return to their usual dietary habits during this washout period. Number of days of the washout period will be recorded.\n\nVisit 5 After the washout period, subjects will return to the study center in the morning after having fasted (other than consuming water) since 11pm the night before. They will have been asked to not brush their teeth or use mouthwash and\u002For other breath fresheners that morning. Anthropomorphic and blood pressure and heart rate recordings will be taken. Saliva will be stored for NO measurement. Blood will be drawn and stored. Urine will be collected and stored.\n\nSubjects will receive one animal-based dinner (food will be provided by Montefiore-Einstein Food Services.) Subjects will then leave the study center and they will consume their usual diet until 5pm. For the rest of the evening until 11pm they will consume only the dinner provided. Water will be the only beverage consumed after 5pm. Dinner should be consumed at 8:30pm, EST. Subjects will text pictures of all they consume (eat or drink) after 5pm to Dr. Ostfeld or to a study representative and s\u002Fhe will have text or verbal contact with the subject at least once that evening. Subjects will fast other than water after 11pm. That night, subjects will do a Rigiscan™ assessment overnight at their home. The time the subject goes to bed and the time the subject wakes up for the day should be recorded. The subject agrees to be in bed with Rigiscan™ on (other than for emergency or needed trips to the bathroom) for at least seven hours.\n\nVisit 6 Subjects will return to the study center the morning after the Rigiscan™ assessment and bring the Rigiscan™ device with them. They will have been asked to not brush their teeth or use mouthwash and\u002For other breath fresheners that morning. Anthropomorphic and blood pressure and heart rate recordings will be taken. Saliva will be stored for NO measurement. Blood will be drawn and stored. Urine will be collected and stored.\n\nSubjects will then receive one full day of animal-based meals (food will be provided by Montefiore-Einstein Food Services.) Subjects will be encouraged to eat breakfast at the study center after the initial anthropomorphic measures are made, saliva is obtained, and blood is drawn. Subjects will text pictures of all they consume during that day to Dr. Ostfeld and\u002For to a study representative and s\u002Fhe will have text or verbal contact with the subject at least twice during that day. Dinner should be consumed at 8:30pm, EST. Subjects will fast other than water after 11pm. That night, subjects will do a Rigiscan™ assessment overnight at their home. Black coffee and\u002For tea is permitted only before noon. The time the subject goes to bed and the time the subject wakes up for the day should be recorded. The subject agrees to be in bed with Rigiscan™ on (other than for emergency or needed trips to the bathroom) for at least seven hours.\n\nVisit 7 (End of Study) Subjects will return to the study center the morning after the Rigiscan™ assessment and bring the Rigiscan™ device with them. They will have been asked to not brush their teeth or use mouthwash and\u002For other breath fresheners that morning. Anthropomorphic and blood pressure and heart rate recordings will be taken. Saliva will be stored for NO measurement. Blood will be drawn and stored. Urine will be collected and stored.\n\nSequence Two:\n\nSequence Two is identical to Sequence One, except that the order of the plant-based and animal-based meals is reversed.",[19],"Erectile Dysfunction",[21,22,23,24],"Diet","Erectile function","Plant-based","Animal-based","INTERVENTIONAL","PREVENTION",[28],"NA",{"count":30,"type":31},46,"ESTIMATED",[33,38],{"type":14,"name":34,"description":35,"armGroupLabels":36},"Animal based diet","Food will be provided by Montefiore-Einstein Food Services",[37],"Animal-based arm",{"type":14,"name":39,"description":35,"armGroupLabels":40},"Plant based diet",[41],"Plant-based arm",[43],{"measure":44,"description":45,"timeFrame":46},"Percent of time ≥60% erect during overnight Rigiscan™ use after 4 meals.","The first 5 minutes of Rigiscan™ recording is discarded. Erection time is the total time (in minutes) when penile rigidity is ≥ 60% at both the tip and base of the penis with a concurrent increase in penile tumescence at both the tip and base of the penis compared to baseline tumescence as measured by Rigiscan™ during overnight Rigiscan™ use, divided by the total time (in minutes) of overnight Rigiscan™ use. Overnight Rigiscan™ use time is defined as starting 5 minutes after the start of the Rigiscan™ recording and the end of Rigiscan™ use is defined as the last time the tip or base was \\>=10% rigid with a corresponding concurrent increase in penile tumescence at the tip or base compared to baseline tumesence. This total time window from start to end is the Rigiscan™ use time.","During overnight Rigiscan™ use directly after consuming the 4 meals. (The second night of Rigiscan™ use).",[48,52,56],{"measure":49,"description":50,"timeFrame":51},"Percent of time ≥60% erect during overnight Rigiscan™ use after 1 meal.","The first 5 minutes of Rigiscan™ recording is discarded. Erection time is the total time (in minutes) when penile rigidity is ≥ 60% at both the tip and base of the penis with a concurrent increase in penile tumescence at both the tip and base of the penis compared to baseline tumescence as measured by Rigiscan™ during overnight Rigiscan™ use, divided by the total time (in minutes) of overnight Rigiscan™ use. Overnight Rigiscan™ use time is defined as starting 5 minutes after the start of the Rigiscan™ recording and the end of Rigiscan™ use is defined as the last time the tip or base was \\>=10% rigid with a corresponding concurrent increase in penile tumescence at the tip or base compared to baseline tumesence. This total time window from start to end is the Rigiscan™ use time","During overnight Rigiscan™ use directly after consuming 1 meal. (The first night of Rigiscan™ use).",{"measure":53,"description":54,"timeFrame":55},"Percent of time ≥60% erect during overnight Rigiscan™ use after 4 meals, where each erection lasts >=5 minutes as measured by Rigiscan™","The first 5 minutes of Rigiscan™ recording is discarded. Erection time is the total time (in minutes) when penile rigidity is ≥ 60% at both the tip and the base of the penis with a concurrent increase in penile tumescence at both the tip and base of the penis compared to baseline tumescence, and the erection lasts \\>= 5 minutes, as measured by Rigiscan™ during overnight Rigiscan™ use, divided by the total time (in minutes) of overnight Rigiscan™ use. Overnight Rigiscan™ use time is defined as starting 5 minutes after the start of the Rigiscan™ recording and the end of Rigiscan™ use is defined as the last time the tip or base was \\>=10% rigid with a corresponding concurrent increase in penile tumescence at the tip or base compared to baseline tumesence. This total time window from start to end is the Rigiscan™ use time.","During overnight Rigiscan™ use directly after consuming 4 meals. (The second night of Rigiscan™ use).",{"measure":57,"description":54,"timeFrame":51},"Percent of time ≥60% erect during overnight Rigiscan™ use after 1 meal, where each erection lasts >=5 minutes as measured by Rigiscan™","MALE","18 Years","35 Years",true,{"inclusion":63,"exclusion":85,"raw_text":110},[64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84],"Subject provides written informed consent and HIPAA authorization in English before any study procedures are conducted.","Subject is taking no medical therapy other than: prn MDIs, medication(s) for anxiety, depression, and\u002For ADHD (these medications include, but are not limited to, SSRIs, SNRIs, Stimulants), no change in supplements if applicable.","IIEF score greater or equal to 22","Subject will have had penile-sexual intercourse (either vaginal or anal penetration) within 12 weeks of enrollment.","Male aged 18-35 years old","Lives within commuting distance of Montefiore Health System","Subject's significant other (if applicable) agrees to support the subject during the study","Subject agrees to photograph and share all items consumed\u002Fdrunk during the dietary intervention","Subject agrees to avoid all illicit drugs, NSAIDS, and alcohol for at least two days prior to Rigiscan™ recording and on the days and nights of Rigiscan™ recording","Subject agrees to refrain from sexual activity for at least 24 hours prior to Rigiscan™ placement and to have no sexual activity on the days and nights of Rigiscan™ recording.","Subject agrees to not view, read, or otherwise consume erotic or pornographic material for 24 hours prior to both the days and nights of Rigiscan™ recording and on the days and nights of Rigiscan™ recording.","Subject agrees to not have an orgasm for 24 hours prior to both the days and nights of RigiscanTM recording and on the days and nights of Rigiscan™ recording.","Subject agrees to come to Montefiore to undergo Rigiscan™ training","Subject agrees to only consume\u002Fdrink permitted food\u002Fbeverages.","Subject agrees to attend all in person visits at Montefiore, to begin fasting at 11pm the night before each visit, and to undergo all blood draws\u002Fsalivary\u002Fother testing.","Subject agrees to not use mouthwash or mouth rinses or intentionally spit for the entire duration of the study. Subjects will be asked to refrain from using mouthwash for at least 2 days prior to enrollment. Subject agrees to not brush his teeth in the morning of the day of each study visit. Tooth brushing is otherwise permissible.","BMI \\\u003C30, BMI \\>=18.5, weight \\>110 lbs.","Subject agrees to comply with the study procedures and visits.","Subject exercises for at least 15 minutes at least two times per week","If exercise is done, subjects will exercise for the same amount of time and at a similar intensity each day of Rigiscan™ testing. Otherwise, no exercise will be performed on Rigiscan™ days.","If enrolled, subjects agree to not modify their dietary habits throughout the duration of the study other than during the two evenings and two full days when food is provided.",[86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109],"Relevant dietary allergy","Vegetarian or Vegan dietary pattern","History of an eating disorder and\u002For food addiction","Hypertension and or history of hypertension with or without medical treatment. Systolic blood pressure \\> 150mmHg and\u002For diastolic blood pressure \\>100mmHg on Visit one. Heart rate \\>99 on Visit one. Systolic blood pressure \\\u003C 85mmHg and\u002For diastolic blood pressure \\\u003C 50mmHg on Visit one. Heart rate \\\u003C 35 on Visit one.","BMI \\>=30, BMI \\\u003C18.5, or weight \\\u003C= 110lbs","Known chronic medical disease other than non-inflammatory musculoskeletal disease, asthma, anxiety, depression, and\u002For ADHD.","History of kidney disease or hyperkalemia","Subject has received an investigational drug within 30 days prior to signing consent","Erectile dysfunction","Has any condition (e.g., psychiatric illness) or situation that, in the investigator's opinion, may confound the study results, or may interfere significantly with the patient's ability to adhere with study procedures","Currently undergoing treatment for Peyronie's Disease","Abnormal Testosterone or Thyroid Stimulating Hormone level","Treated hypogonadism or hypothyroidism","Planned travel during the study","The subject is trans-gender","History of substance abuse in the last 12 months","Illicit drug use, smoking, or vaping within 4 weeks","Upper respiratory illness within two weeks on screening","If profession requires being on call, no overnight or on call duties during the study","Subject reports any communicable skin or venereal disease","Subject reports rash or lesion on the penis or surrounding area.","STOP-Bang score \\> 2","Having the diagnosis of Restless Leg Syndrome.","Having insomnia as defined by: Subject with insomnia would have difficulty initiating or maintaining sleep (30 minutes or more at sleep initiation or 30 minutes or more to fall back asleep if wakes during the night). The above occurs at least 3 times per week for at least 1 month. Furthermore, there must be adequate opportunity for sleep and there must be associated morbidity (feels tired during the day). Definition based on: The International Classification of Sleep Disorders - Third Edition (ICSD-3), 2014.","Inclusion Criteria:\n\n* Subject provides written informed consent and HIPAA authorization in English before any study procedures are conducted.\n* Subject is taking no medical therapy other than: prn MDIs, medication(s) for anxiety, depression, and\u002For ADHD (these medications include, but are not limited to, SSRIs, SNRIs, Stimulants), no change in supplements if applicable.\n\nThe anxiety, depression, and\u002For ADHD will have been controlled (per report of subject) for the last 6 months.\n\n* IIEF score greater or equal to 22\n* Subject will have had penile-sexual intercourse (either vaginal or anal penetration) within 12 weeks of enrollment.\n* Male aged 18-35 years old\n* Lives within commuting distance of Montefiore Health System\n* Subject's significant other (if applicable) agrees to support the subject during the study\n* Subject agrees to photograph and share all items consumed\u002Fdrunk during the dietary intervention\n* Subject agrees to avoid all illicit drugs, NSAIDS, and alcohol for at least two days prior to Rigiscan™ recording and on the days and nights of Rigiscan™ recording\n* Subject agrees to refrain from sexual activity for at least 24 hours prior to Rigiscan™ placement and to have no sexual activity on the days and nights of Rigiscan™ recording.\n* Subject agrees to not view, read, or otherwise consume erotic or pornographic material for 24 hours prior to both the days and nights of Rigiscan™ recording and on the days and nights of Rigiscan™ recording.\n* Subject agrees to not have an orgasm for 24 hours prior to both the days and nights of RigiscanTM recording and on the days and nights of Rigiscan™ recording.\n* Subject agrees to come to Montefiore to undergo Rigiscan™ training\n* Subject agrees to only consume\u002Fdrink permitted food\u002Fbeverages.\n* Subject agrees to attend all in person visits at Montefiore, to begin fasting at 11pm the night before each visit, and to undergo all blood draws\u002Fsalivary\u002Fother testing.\n* Subject agrees to not use mouthwash or mouth rinses or intentionally spit for the entire duration of the study. Subjects will be asked to refrain from using mouthwash for at least 2 days prior to enrollment. Subject agrees to not brush his teeth in the morning of the day of each study visit. Tooth brushing is otherwise permissible.\n* BMI \\\u003C30, BMI \\>=18.5, weight \\>110 lbs.\n* Subject agrees to comply with the study procedures and visits.\n* Subject exercises for at least 15 minutes at least two times per week\n* If exercise is done, subjects will exercise for the same amount of time and at a similar intensity each day of Rigiscan™ testing. Otherwise, no exercise will be performed on Rigiscan™ days.\n* If enrolled, subjects agree to not modify their dietary habits throughout the duration of the study other than during the two evenings and two full days when food is provided.\n\nExclusion Criteria:\n\n* Relevant dietary allergy\n* Vegetarian or Vegan dietary pattern\n* History of an eating disorder and\u002For food addiction\n* Hypertension and or history of hypertension with or without medical treatment. Systolic blood pressure \\> 150mmHg and\u002For diastolic blood pressure \\>100mmHg on Visit one. Heart rate \\>99 on Visit one. Systolic blood pressure \\\u003C 85mmHg and\u002For diastolic blood pressure \\\u003C 50mmHg on Visit one. Heart rate \\\u003C 35 on Visit one.\n* BMI \\>=30, BMI \\\u003C18.5, or weight \\\u003C= 110lbs\n* Known chronic medical disease other than non-inflammatory musculoskeletal disease, asthma, anxiety, depression, and\u002For ADHD.\n\nSubjects who have had changes in the dosage or type of their medication(s) for anxiety, depression, and\u002For ADHD within 3 months of enrollment.\n\nSubjects who have scheduled or planned medication and\u002For medication dose changes during the study period. These medication changes include the initiation of a new medication, discontinuation of a medication, modification of medication dose, and\u002For the route of administration of a medication.\n\nSubjects who are taking benzodiazepines and\u002For beta blockers\n\n* History of kidney disease or hyperkalemia\n* Subject has received an investigational drug within 30 days prior to signing consent\n* Erectile dysfunction\n* Has any condition (e.g., psychiatric illness) or situation that, in the investigator's opinion, may confound the study results, or may interfere significantly with the patient's ability to adhere with study procedures\n* Currently undergoing treatment for Peyronie's Disease\n* Abnormal Testosterone or Thyroid Stimulating Hormone level\n* Treated hypogonadism or hypothyroidism\n* Planned travel during the study\n* The subject is trans-gender\n* History of substance abuse in the last 12 months\n* Illicit drug use, smoking, or vaping within 4 weeks\n* Upper respiratory illness within two weeks on screening\n* If profession requires being on call, no overnight or on call duties during the study\n* Subject reports any communicable skin or venereal disease\n* Subject reports rash or lesion on the penis or surrounding area.\n* STOP-Bang score \\> 2\n* Having the diagnosis of Restless Leg Syndrome.\n* Having insomnia as defined by: Subject with insomnia would have difficulty initiating or maintaining sleep (30 minutes or more at sleep initiation or 30 minutes or more to fall back asleep if wakes during the night). The above occurs at least 3 times per week for at least 1 month. Furthermore, there must be adequate opportunity for sleep and there must be associated morbidity (feels tired during the day). Definition based on: The International Classification of Sleep Disorders - Third Edition (ICSD-3), 2014.",[112],"ADULT",[114],{"facility":115,"status":8,"city":116,"state":117,"zip":118,"country":119,"contacts":120,"geoPoint":126},"Montefiore Medical Center, Department of Medicine, Division of Cardiology","The Bronx","New York","10467","United States",[121],{"name":122,"role":123,"phone":124,"email":125},"Robert J Ostfeld, MD, MS","CONTACT","718-920-8011","rostfeld@montefiore.org",{"lat":127,"lon":128},40.84985,-73.86641,[130],{"name":131,"role":123,"phone":132,"email":133},"Robert Ostfeld, MD","718-920-5197","ROSTFELD@montefiore.org",[135],{"name":131,"affiliation":13,"role":136},"PRINCIPAL_INVESTIGATOR",[138,142,145,148,151,154,157,160,163,166,169,172,175,178,181,184,187],{"pmid":139,"type":140,"citation":141},"8254833","BACKGROUND","Feldman HA, Goldstein I, Hatzichristou DG, Krane RJ, McKinlay JB. Impotence and its medical and psychosocial correlates: results of the Massachusetts Male Aging Study. J Urol. 1994 Jan;151(1):54-61. doi: 10.1016\u002Fs0022-5347(17)34871-1.",{"pmid":143,"type":140,"citation":144},"19181648","Nehra A. Erectile dysfunction and cardiovascular disease: efficacy and safety of phosphodiesterase type 5 inhibitors in men with both conditions. Mayo Clin Proc. 2009 Feb;84(2):139-48. doi: 10.4065\u002F84.2.139.",{"pmid":146,"type":140,"citation":147},"16414947","Thompson IM, Tangen CM, Goodman PJ, Probstfield JL, Moinpour CM, Coltman CA. Erectile dysfunction and subsequent cardiovascular disease. JAMA. 2005 Dec 21;294(23):2996-3002. doi: 10.1001\u002Fjama.294.23.2996.",{"pmid":149,"type":140,"citation":150},"9036757","Vogel RA, Corretti MC, Plotnick GD. Effect of a single high-fat meal on endothelial function in healthy subjects. Am J Cardiol. 1997 Feb 1;79(3):350-4. doi: 10.1016\u002Fs0002-9149(96)00760-6.",{"pmid":152,"type":140,"citation":153},"10609824","Ong PJ, Dean TS, Hayward CS, Della Monica PL, Sanders TA, Collins P. Effect of fat and carbohydrate consumption on endothelial function. Lancet. 1999 Dec 18-25;354(9196):2134. doi: 10.1016\u002Fs0140-6736(99)03374-7.",{"pmid":155,"type":140,"citation":156},"12499333","Esposito K, Nappo F, Giugliano F, Giugliano G, Marfella R, Giugliano D. Effect of dietary antioxidants on postprandial endothelial dysfunction induced by a high-fat meal in healthy subjects. Am J Clin Nutr. 2003 Jan;77(1):139-43. doi: 10.1093\u002Fajcn\u002F77.1.139.",{"pmid":158,"type":140,"citation":159},"17921366","Shimabukuro M, Chinen I, Higa N, Takasu N, Yamakawa K, Ueda S. Effects of dietary composition on postprandial endothelial function and adiponectin concentrations in healthy humans: a crossover controlled study. Am J Clin Nutr. 2007 Oct;86(4):923-8. doi: 10.1093\u002Fajcn\u002F86.4.923.",{"pmid":161,"type":140,"citation":162},"20460711","Sakakibara S, Murakami R, Takahashi M, Fushimi T, Murohara T, Kishi M, Kajimoto Y, Kitakaze M, Kaga T. Vinegar intake enhances flow-mediated vasodilatation via upregulation of endothelial nitric oxide synthase activity. Biosci Biotechnol Biochem. 2010;74(5):1055-61. doi: 10.1271\u002Fbbb.90953. Epub 2010 May 7.",{"pmid":164,"type":140,"citation":165},"16395320","Esposito K, Ciotola M, Giugliano F, De Sio M, Giugliano G, D'armiento M, Giugliano D. Mediterranean diet improves erectile function in subjects with the metabolic syndrome. Int J Impot Res. 2006 Jul-Aug;18(4):405-10. doi: 10.1038\u002Fsj.ijir.3901447. Epub 2006 Jan 5.",{"pmid":167,"type":140,"citation":168},"19694925","Wing RR, Rosen RC, Fava JL, Bahnson J, Brancati F, Gendrano Iii IN, Kitabchi A, Schneider SH, Wadden TA. Effects of weight loss intervention on erectile function in older men with type 2 diabetes in the Look AHEAD trial. J Sex Med. 2010 Jan;7(1 Pt 1):156-65. doi: 10.1111\u002Fj.1743-6109.2009.01458.x. Epub 2009 Aug 17.",{"pmid":170,"type":140,"citation":171},"21911624","Gupta BP, Murad MH, Clifton MM, Prokop L, Nehra A, Kopecky SL. The effect of lifestyle modification and cardiovascular risk factor reduction on erectile dysfunction: a systematic review and meta-analysis. Arch Intern Med. 2011 Nov 14;171(20):1797-803. doi: 10.1001\u002Farchinternmed.2011.440. Epub 2011 Sep 12.",{"pmid":173,"type":140,"citation":174},"26762373","Cassidy A, Franz M, Rimm EB. Dietary flavonoid intake and incidence of erectile dysfunction. Am J Clin Nutr. 2016 Feb;103(2):534-41. doi: 10.3945\u002Fajcn.115.122010. Epub 2016 Jan 13.",{"pmid":176,"type":140,"citation":177},"12789391","Yaman O, Tokath Z, Inal T, Anafarta K. Effect of sildenafil on nocturnal erections of potent men. Int J Impot Res. 2003 Apr;15(2):117-21. doi: 10.1038\u002Fsj.ijir.3900978.",{"pmid":179,"type":140,"citation":180},"10318772","Corbin JD, Francis SH. Cyclic GMP phosphodiesterase-5: target of sildenafil. J Biol Chem. 1999 May 14;274(20):13729-32. doi: 10.1074\u002Fjbc.274.20.13729. No abstract available.",{"pmid":182,"type":140,"citation":183},"16422962","Greenstein A, Chen J, Salonia A, Sofer M, Matzkin H, Montorsi F. Does sildenafil enhance quality of nocturnal erections in healthy young men? A NPT-RigiScan study. J Sex Med. 2004 Nov;1(3):314-7. doi: 10.1111\u002Fj.1743-6109.04045.x.",{"pmid":185,"type":140,"citation":186},"2621154","Burris AS, Banks SM, Sherins RJ. Quantitative assessment of nocturnal penile tumescence and rigidity in normal men using a home monitor. J Androl. 1989 Nov-Dec;10(6):492-7. doi: 10.1002\u002Fj.1939-4640.1989.tb00148.x.",{"pmid":188,"type":140,"citation":189},"26378880","Chung F, Abdullah HR, Liao P. STOP-Bang Questionnaire: A Practical Approach to Screen for Obstructive Sleep Apnea. Chest. 2016 Mar;149(3):631-8. doi: 10.1378\u002Fchest.15-0903. Epub 2016 Jan 12.",[],{"nct_id":4,"conditions":192,"biomarkers":193},[19],[194,195],"Testosterone","Thyroid-Stimulating Hormone",{"nct_id":4,"found":61,"summary":197,"prompt_version":207},{"design":198,"status":199,"heading":200,"summary":201,"follow_up":202,"word_count":203,"commitments":204,"compensation":205,"drugs_mentioned":206},"This is an interventional study, meaning participants will receive a specific intervention (either an animal-based or plant-based diet). It plans to enroll 46 men.","completed","Dietary Patterns and Erectile Function Study","This study aims to understand if different eating patterns affect erectile function in healthy men. Researchers will provide participants with either an animal-based diet or a plant-based diet. The main goal is to see how much time participants spend with at least 60% erection during overnight Rigiscan™ (a device that measures erections during sleep) use after eating four meals on their assigned diet. You may be able to join if you are a man between 18 and 35 years old and have normal erectile function. The study is looking to enroll 46 participants. The study status is currently unclear, so it's not known if they are actively recruiting.","Erectile function will be measured during overnight Rigiscan™ use directly after consuming the four meals, specifically on the second night of Rigiscan™ use.",108,"You will undergo a screening visit including questionnaires, medical history, physical measurements, and blood tests. If eligible, you will be randomized to one of two diet groups and will have food provided. You will also use a Rigiscan™ device for overnight measurements.","Not stated in the trial record.",[],"v2"]