[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"epigastric-hernia-repair\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:epigastric-hernia-repair":41},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":5},"100629583",false,"NCT07476560","Evaluating the Efficacy of Suture Mesh vs. Planar Mesh in Ventral Hernia Treatment","Mesh Matters: Evaluating the Efficacy of Suture Mesh vs. Planar Mesh in Ventral Hernia Treatment - a Randomized, Blinded Multicenter Study","MeMa","Inclusion Criteria:\n\n* Ventral hernia (maximum size 3 × 3 cm) measured with Ultrasound or CT.\n* Participants must be eligible for surgical repair using either mesh-suture or planar mesh\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years.\n* Acute (emergent) operation.\n* Pregnancy.\n* Women with plans for future pregnancies.\n* Withdrawal of informed consent during admission.","ALL","18 Years",{"count":19,"type":20},280,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to investigate whether mesh-suture affects wound complication rates, patient-reported quality of life, and operation time in adult patients undergoing surgery for small ventral hernias.\n\nThe main questions it aims to answer are:\n\nDoes mesh-suture reduce wound complication rates compared to planar mesh? Does mesh-suture improve patient-reported quality of life(QoL) and affect operation time compared to planar mesh?\n\nComparison group:\n\nResearchers will compare standard treatment with planar mesh to the interventional treatment with mesh-suture to see whether mesh-suture leads to fewer complications, better quality of life, and shorter operation time.\n\nParticipants will:\n\nBe randomized to receive either planar mesh or mesh-suture during hernia repair surgery.\n\nUndergo standardized preoperative assessment, including baseline data and QoL scoring.\n\nAttend a postoperative visit on day 7-13 for wound inspection and ultrasound. Complete QoL assessments at 90 days (telephone follow-up). Have operation time recorded and medical records reviewed for readmissions within 90 days.",[26,27,28],"Abdominal Wall Hernia","Umbilical Hernia Repair","Epigastric Hernia Repair","RECRUITING","2026-03-12",{"date":32,"type":33},"2026-03-17","ACTUAL",{"date":35,"type":33},"2026-01-05",{"date":37,"type":20},"2032-12-31",{"name":39,"class":40},"Regionshospital Nordjylland","OTHER_GOV",""]