[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT06043557":3,"trial-entities:NCT06043557":81,"trial-summary:NCT06043557":84},{"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":21,"study_type":24,"primary_purpose":25,"phases":26,"enrollment_info":28,"interventions":31,"primary_outcomes":39,"secondary_outcomes":44,"sex":49,"minimum_age":50,"maximum_age":51,"healthy_volunteers":15,"eligibility_criteria":52,"std_ages":62,"locations":65,"central_contacts":74,"overall_officials":75,"references":79,"see_also_links":80},"NCT06043557","IRB00100958","Patient Satisfaction and Reflection on Drain Placement","Patient Satisfaction and Reflection on Drain Placement in Abdominoplasty and Panniculectomy","ENROLLING_BY_INVITATION","2026-12","2025-08","2025-08-24","2024-01-01","Wake Forest University Health Sciences","OTHER",false,"The purpose of this research study is to evaluate the ideal drain placement in patients undergoing abdominoplasty or panniculectomy. There are currently no patient reported outcome measurements on ideal drain placement and this study aims to collect objective and patient reported measures to standardize ideal drain placement.\n\nIn this study a medially and laterally placed drain will be compared to each other in each study participant. In this study subject will have two drains. One will be lateral and one medial. The drains will be secured and dressed in the same manner. At subjects planned post-operative visits, subjects will be asked to complete surveys to evaluate their experience with the drains. This study will not require additional clinic visits for study purposes.","The primary goal of this proposal is to assess patient perspectives and satisfaction with the location of their drains after abdominoplasty and\u002For panniculectomy. This will be conducted as a prospective observational trial, where patients with scheduled abdominoplasty and\u002For panniculectomy will be invited to participate. Patients will be randomized to either A) left side lateral and right side medial or B) right side lateral with left side medial. Randomization will occur before study initiation with group A or group B being assigned to a study enrollment number.",[19,20],"Abdominoplasty","Panniculectomy",[19,22,23],"plastic surgery","panniculectomy","INTERVENTIONAL","TREATMENT",[27],"NA",{"count":29,"type":30},50,"ESTIMATED",[32],{"type":33,"name":34,"description":35,"armGroupLabels":36},"PROCEDURE","Drain Placement","Surgical placement of drain based on subject randomization.",[37,38],"left side lateral and right side medial","right side lateral with left side medial",[40],{"measure":41,"description":42,"timeFrame":43},"Patient preference of surgical drain placement","Patients will complete a survey about their experience with the pertinent securement method\u002Fdrain site - questions are essay style without a score or range\n\nIn the survey we created the level of negative factors (pulling, tugging, pain) as well as positive (ease of drain care, ease of personal hygiene) will be on a 1-100 scale. Therefore each side will get a conglomerate score of the following:\n\nTotal score = positive scores (average) - negative scores (average)\n\nThis result will be tabulated for each patient and used as a group analysis for preference. (Average scores for each side from all patients compared to one another.)","1 week post surgery",[45],{"measure":46,"description":47,"timeFrame":48},"Number of days until drain removed","tracking number of days","day of surgery up to 10 days","ALL","18 Years",null,{"inclusion":53,"exclusion":58,"raw_text":61},[54,55,56,57],"age 18 or older","patient of Department of Plastic and Reconstructive Surgery","able to sign English language Consent form","undergoing either abdominoplasty and\u002For panniculectomy.",[59,60],"Patients with unilateral drain placement, unable to sign English language consent form","Patient under the age of 18.","Inclusion Criteria:\n\n* age 18 or older\n* patient of Department of Plastic and Reconstructive Surgery\n* able to sign English language Consent form\n* undergoing either abdominoplasty and\u002For panniculectomy.\n\nExclusion Criteria:\n\n* Patients with unilateral drain placement, unable to sign English language consent form\n* Patient under the age of 18.",[63,64],"ADULT","OLDER_ADULT",[66],{"facility":13,"city":67,"state":68,"zip":69,"country":70,"geoPoint":71},"Winston-Salem","North Carolina","27157","United States",{"lat":72,"lon":73},36.09986,-80.24422,[],[76],{"name":77,"affiliation":13,"role":78},"Adam Katz, MD","PRINCIPAL_INVESTIGATOR",[],[],{"nct_id":4,"conditions":82,"biomarkers":83},[19,20],[],{"nct_id":4,"found":15,"summary":51,"prompt_version":51}]