[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100649567":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":38,"locations":47,"responsibleParty":62,"collaborators":26,"id":66,"slug":67,"hasResults":68,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":72,"eligibilityCriteria":73,"healthyVolunteers":68,"sex":74,"minAge":75,"maxAge":26,"enrollmentInfo":76,"targetDuration":26,"studyType":79,"phases":80,"briefSummary":82,"conditions":83,"keywords":87,"overallStatus":50,"whyStopped":26,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":104},{"fullName":5,"class":6},"Başakşehir Çam & Sakura City Hospital","OTHER_GOV",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Subcutaneous Drain","EXPERIMENTAL","Participants allocated to this arm will receive prophylactic closed-suction subcutaneous drainage after midline laparotomy and before skin closure. Subcutaneous tissue approximation will be performed with interrupted 2\u002F0 Vicryl sutures. The drain will be removed when the 24-hour drainage volume is less than 30 mL, unless earlier or later removal is clinically indicated.",[13],"Procedure: Prophylactic subcutaneous closed-suction drainage",{"label":15,"type":16,"description":17,"interventionNames":18},"No Subcutaneous Drain","ACTIVE_COMPARATOR","Participants allocated to this arm will undergo standard surgical closure without prophylactic subcutaneous drainage. Subcutaneous tissue approximation will be performed with interrupted 2\u002F0 Vicryl sutures.",[19],"Procedure: Standard closure without subcutaneous drainage",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","Prophylactic subcutaneous closed-suction drainage","Placement of a closed-suction drain in the subcutaneous tissue before skin closure in patients with intraoperative subcutaneous tissue thickness of 2.5 cm or greater.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Standard closure without subcutaneous drainage","Standardized subcutaneous tissue approximation and skin closure without placement of a prophylactic subcutaneous drain.",[15],[32,35],{"name":33,"affiliation":5,"role":34},"MAHMUT YASSA, MD","PRINCIPAL_INVESTIGATOR",{"name":36,"affiliation":5,"role":37},"Bora Taşpınar, MD","STUDY_DIRECTOR",[39,44],{"name":40,"role":41,"phone":42,"phoneExt":26,"email":43},"MAHMUT yassa, MD","CONTACT","+905396635484","mahmut_yassa@hotmail.com",{"name":36,"role":41,"phone":45,"phoneExt":26,"email":46},"+905053946331","borataspinar@gmail.com",[48],{"facility":49,"status":50,"city":51,"state":26,"zip":26,"country":52,"countryCode":26,"cosmosGeoPoint":53,"geoPoint":58,"contacts":59},"Başakşehir Çam and Sakura City Hospital","RECRUITING","Istanbul","Turkey (Türkiye)",{"type":54,"coordinates":55},"Point",[56,57],28.94966,41.01384,{"lat":57,"lon":56},[60],{"name":61,"role":41,"phone":42,"phoneExt":26,"email":43},"mahmut yassa",{"type":63,"investigatorFullName":64,"investigatorTitle":65,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"SPONSOR_INVESTIGATOR","Mahmut Yassa","Gynecologic Oncology Specialist","100649567","prophylactic-subcutaneous-drainage-after-gynecologic-oncology-midline-laparotomy-100649567",false,"NCT07735962","Prophylactic Subcutaneous Drainage After Gynecologic Oncology Midline Laparotomy","Effect of Prophylactic Subcutaneous Drainage on Wound Complications in Patients With Thick Subcutaneous Tissue Undergoing Midline Laparotomy for Gynecologic Oncology Surgery: A Randomized Controlled Trial","SCDRAIN-GO","Inclusion Criteria:\n\n* Female participants aged 18 years or older\n* Undergoing midline laparotomy for gynecologic oncology surgery\n* Intraoperative subcutaneous tissue thickness of 2.5 cm or greater, measured at the thickest part of the incision\n* Able and willing to provide written informed consent before surgery\n\nExclusion Criteria:\n\n* Emergency surgery\n* Active infection before surgery\n* Severe immunosuppression\n* Refusal to provide written informed consent","FEMALE","18 Years",{"count":77,"type":78},334,"ESTIMATED","INTERVENTIONAL",[81],"NA","The goal of this clinical trial is to learn whether placing a small drain under the skin can help prevent wound problems after gynecologic oncology surgery in adult women with a thick layer of tissue under the skin.\n\nThe main question it aims to answer is:\n\nDoes a small drain placed under the skin lower the number of wound complications within 30 days after surgery?\n\nResearchers will compare two groups:\n\nParticipants in one group will have a small closed-suction drain placed under the skin before the skin is closed.\n\nParticipants in the other group will not have a drain placed under the skin.\n\nAll participants will have midline abdominal surgery. During surgery, the surgeon will measure the thickness of the tissue under the skin. Participants with a thickness of 2.5 cm or more will be randomly assigned to one of the two groups.\n\nIn both groups, the tissue under the skin will be closed in a standard way using separate 2\u002F0 Vicryl stitches. Participants in the drain group will have the drain removed when the amount of fluid collected in 24 hours is less than 30 mL, unless the surgeon decides that earlier or later removal is needed.\n\nParticipants will be followed for 30 days after surgery to check for wound problems such as infection, wound separation, fluid collection, blood collection, or the need for extra wound care or another procedure.",[84,85,86],"Wound Complication","Surgical Site Infection (SSI)","Gynecologic Cancers",[88,89,90,91,92,93,94],"subcutaneous drain","gynecologic oncology","midline laparotomy","wound complication","surgical site infection","subcutaneous tissue thickness","randomized controlled trial","2026-07-29",{"date":97,"type":98},"2026-07-30","ACTUAL",{"date":100,"type":98},"2026-07-20",{"date":102,"type":78},"2028-03-01",{"name":64,"class":6},1]