[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT04235764":3,"trial-entities:NCT04235764":100,"trial-summary:NCT04235764":104},{"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":26,"primary_purpose":15,"phases":27,"enrollment_info":28,"interventions":31,"primary_outcomes":42,"secondary_outcomes":47,"sex":51,"minimum_age":52,"maximum_age":53,"healthy_volunteers":54,"eligibility_criteria":55,"std_ages":65,"locations":68,"central_contacts":83,"overall_officials":92,"references":95,"see_also_links":96},"NCT04235764","200020","En-bloc Transurethral Resection of Bladder Tumor (En-bloc TURBT) Specimens Using a Redesigned Surgical Resectoscope Device","Ex-Vivo Trial of En-bloc Transurethral Resection of Bladder Tumor (En-bloc TURBT) Specimens Using a Redesigned Surgical Resectoscope Device","RECRUITING","2027-09-30","2026-08-17","2026-09-08","2020-09-09","National Cancer Institute (NCI)","NIH",null,"Background:\n\nBladder cancer is the sixth most common cancer in the United States. The way that doctors remove tumors in bladder surgeries may leave some cancer . Also, many people have their tumors return or progress after surgery. Researchers want to test a modified device. It might tell doctors more about bladder tumors.\n\nObjective:\n\nTo see if using a modified standard device with bladder surgery can provide better information about tumors in bladder specimens.\n\nEligibility:\n\nPeople ages 18 and older who need to have their bladder removed at the NIH.\n\nDesign:\n\nParticipants will be screened with:\n\nMedical and prior surgical history\n\nReview of existing MRI, x-ray, or CT scans\n\nReview of existing specimens and reports\n\nPregnancy test for women of childbearing age\n\nCT or MRI: Participants will lie in a machine. The machine will take pictures of their body.\n\nParticipants will have bladder surgery. This will occur in the same way as if they did not take part in this study. A member of the research team will cut the removed bladder using the modified device. This will most likely be done on a separate back table in the operating room. The bladder and samples after cutting will be sent out for review. The will occur just as it would if the participants were not in this study. The only difference is the way that the specimen is prepared for review.\n\nParticipants follow-up care will occur per standard of care. Or it will occur as part of any other study in which they might also be enrolled.","Background:\n\n* Bladder cancer is the sixth most common cancer in the United States, disproportionately affecting more men than women.\n* The gold standard for the surgical treatment and diagnosis of non-muscle invasive bladder cancer is transurethral resection of bladder tumors (TURBT).\n* TURBT requires the fragmentation of bladder tumors and piecemeal removal of these tumors.\n* TURBT leads to loss of histopathologic information - including tumor orientation, size, and margin status - which may compromise outcomes and risk tumor seeding within the bladder.\n* Given these multiple problems with TURBT we are testing some modifications to the current resectoscope device and the effect of these modifications on the quality of TURBT specimens produced.\n* The redesigned resectoscope device will be tested ex-vivo on cystectomy specimens to avoid risks to patient safety.\n\nObjectives:\n\nThe primary objective of this study is to determine if resectoscope device modification can provide improved pathologic standards for the TURBT procedure. An improvement in any of the parameters outlined below will constitute a device improvement in the current resectoscope:\n\n* Presence of three tissue layers within the tumor specimens containing bladder mucosa, lamina propria, and portions of the muscularis.\n* Information regarding tumor margin, assessed as the ability to ascertain if tumor is present at the margin of the resection.\n\nEligibility:\n\n* Medical condition requiring surgical removal of the bladder\n* Men and women, age \\>= 18 years\n\nDesign:\n\n* Preclinical tissue acquisition trial, ex vivo, proof-of-concept.\n* Following cystectomy, a modified resectoscope\u002Fredesigned resectoscope will be used to resect areas of tumor from the cystectomy specimens. These resected tumors will be sent with the cystectomy specimen for histopathology to assess the size of resection, depth of resection, and ability to ascertain tumor orientation.\n* The remainder of the cystectomy specimens will undergo traditional histopathology. Histopathologic information from both specimens will be included in the final histopathologic diagnosis to ensure accurate oncology staging.\n* This study will allow for about 2 years of accrual and the accrual ceiling will be set at 25 subjects.",[19],"Bladder Cancer",[21,22,23,24,25],"TURBT","Transurethral Resection of Bladder Tumors","Cystectomy","Modified Resectoscope","Natural History","OBSERVATIONAL",[],{"count":29,"type":30},25,"ESTIMATED",[32,38],{"type":33,"name":34,"description":35,"armGroupLabels":36},"DEVICE","modified resectoscope","The modified resectoscope will be used post cystectomy (En-bloc TURBT) to resect areas of the tumor from the cystectomy specimen. These resected tumors will be sent for histopathology to assess the size of resection, depth of resection, and ability to ascertain tumor orientation and compared to the remainder of the cystectomy specimens to see if the modified resectoscope can provide improved pathologic standards for the TURBT procedure.",[37],"1\u002F Cohort 1",{"type":39,"name":21,"description":40,"armGroupLabels":41},"PROCEDURE","All patients will receive routine surgical transurethral resection of bladder tumors (TURBT).",[37],[43],{"measure":44,"description":45,"timeFrame":46},"Assessment of resectoscope device modification on pathologic standards for the TURBT procedure","-Presence of three tissue layers with in the tumor specimens containing bladder mucosa, lamina propria, and portions of the muscularis.-Information regarding tumor margin, assessed as the ability to ascertain if tumor is present at the margin of the resection.","Time of surgery\u002Fpathologic assessment (7-10 days)",[48],{"measure":49,"description":50,"timeFrame":46},"Assessment for possible bladder perforation in bladder specimens","The rate of occurrence will be described\u002Ftabulated.","ALL","18 Years","120 Years",false,{"inclusion":56,"exclusion":63,"raw_text":64},[57,58,59,60,61,62],"Patients requiring surgical removal of the bladder at the NIH Clinical Center.","Men and women","Age greater than or less than 18 years","Deemed clinically appropriate for the planned surgical procedure.","Ability of subject to understand and the willingness to sign a written informed consent document.","Subjects will be asked to co-enroll in 15-C-0087, \"Care of the Urothelial Cancer Patient and Prospective Collection of Biospecimens from Healthy Volunteers and Urothelial Cancer Patients.\" NOTE: Most participants are expected to already be enrolled in 15-C-0087 prior to entry in this study.",[],"* INCLUSION CRITERIA:\n* Patients requiring surgical removal of the bladder at the NIH Clinical Center.\n\nNOTE: Reasons for need for surgical removal of bladder include cancer or benign condition for which a surgeon determined surgical removal of the bladder is recommended. Patient's with invasive bladder cancer requiring cystectomy are eligible for enrollment. Bladder cancer remains the most common reason for cystectomy. Patients with clinical advanced disease and having other treatments\u002For participating in other trials remain eligible for enrollment in this study.\n\n* Men and women\n* Age greater than or less than 18 years\n* Deemed clinically appropriate for the planned surgical procedure.\n* Ability of subject to understand and the willingness to sign a written informed consent document.\n* Subjects will be asked to co-enroll in 15-C-0087, \"Care of the Urothelial Cancer Patient and Prospective Collection of Biospecimens from Healthy Volunteers and Urothelial Cancer Patients.\" NOTE: Most participants are expected to already be enrolled in 15-C-0087 prior to entry in this study.\n\nEXCLUSION CRITERIA:\n\n\\- Cystectomy during pregnancy would subject the fetus to significant risk of miscarriage or premature labor. For this reason, pregnant women are ineligible for this study.",[66,67],"ADULT","OLDER_ADULT",[69],{"facility":70,"status":8,"city":71,"state":72,"zip":73,"country":74,"contacts":75,"geoPoint":80},"National Institutes of Health Clinical Center","Bethesda","Maryland","20892","United States",[76],{"name":77,"role":78,"phone":79},"For more information at the NIH Clinical Center contact National Cancer Institute Referral Office","CONTACT","888-624-1937",{"lat":81,"lon":82},38.98067,-77.10026,[84,88],{"name":85,"role":78,"phone":86,"email":87},"NCI Medical Oncology Referral Office","(240) 760-6050","ncimo_referrals@nih.gov",{"name":89,"role":78,"phone":90,"email":91},"Raju R Chelluri, M.D.","(240) 858-3700","raju.chelluri@nih.gov",[93],{"name":89,"affiliation":13,"role":94},"PRINCIPAL_INVESTIGATOR",[],[97],{"label":98,"url":99},"NIH Clinical Center Detailed Web Page","https:\u002F\u002Fclinicalstudies.info.nih.gov\u002Fcgi\u002Fdetail.cgi?A_2020-C-0020.html",{"nct_id":4,"conditions":101,"biomarkers":103},[102],"Bladder Carcinoma",[],{"nct_id":4,"found":105,"summary":106,"prompt_version":116},true,{"design":107,"status":108,"heading":109,"summary":110,"follow_up":111,"word_count":112,"commitments":113,"compensation":114,"drugs_mentioned":115},"This is an observational study involving 25 participants. It compares a modified resectoscope to the standard TURBT procedure.","completed","Observational Study of a Modified Resectoscope for Bladder Cancer","This observational study is looking at a modified resectoscope (a surgical tool) used after a cystectomy (surgical removal of the bladder). The goal is to see if this modified device can provide better information about bladder tumors compared to the standard TURBT (transurethral resection of bladder tumors) procedure. Researchers want to know if the modified resectoscope helps doctors get more complete tumor samples, including all tissue layers, which could improve understanding of the cancer. You may be able to join if you are 18 or older and need your bladder removed at the NIH Clinical Center. This study is currently unclear on its recruitment status and plans to enroll 25 participants.","The primary outcome, assessment of the resectoscope modification, will be measured at the time of surgery\u002Fpathologic assessment (7-10 days).",111,"You will receive routine surgical transurethral resection of bladder tumors (TURBT). The modified resectoscope will be used on your removed bladder specimen after surgery.","Not stated in the trial record.",[34,21],"v2"]