[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"tendon-adhesion\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:tendon-adhesion":39},{"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":12,"acronym":4,"eligibilityCriteria":13,"healthyVolunteers":10,"sex":14,"minAge":15,"maxAge":16,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":5},"100571709",false,"NCT06723782","Surgical Release of Hand Tendons with Wrapping of the Released Tendon Using an Amniotic Membrane","Inclusion Criteria:\n\n* Man or woman aged 18 to 65 years old\n* Adhesion of a flexor and\u002For extensor tendon of the hand.\n* Adhesion localized to a single finger.\n* Adhesion that has been present for at least 3 months following primary repair, despite high-quality rehabilitation. Primary repair is defined as the repair of a tendon injury, fracture, crush injury of the finger, infection, etc., leading to the adhesion of the tendon to surrounding tissue.\n* Patient with a total passive range of motion of the proximal and distal interphalangeal joints of at least 150°.\n* Informed and consenting patient.\n* Patient enrolled in a social security plan or a beneficiary of such a plan.\n\nExclusion Criteria:\n\n* Pregnant or breastfeeding woman, or without an effective method of contraception.\n* Patient requiring tenolysis after tendon grafting for the reconstruction of a deep common flexor or after reimplantation.\n* Patient with amputated hand(s).\n* Patient with an untreated fracture or non-union in the affected hand.\n* Patient requiring multiple surgical interventions that may be potential confounding factors, particularly those involving additional incisions.\n* Patient unable to understand rehabilitation or follow the study protocol.\n* Patient with a contraindication to anesthesia.\n* Person deprived of liberty by judicial or administrative decision.\n* Adult subject to legal protection measures or incapable of expressing consent.","ALL","18 Years","65 Years",{"count":18,"type":19},16,"ESTIMATED","INTERVENTIONAL",[22],"PHASE2","The goal of this clinical trial is to evaluate whether an amniotic membrane can function as an effective anti-adhesive barrier following surgical release of tendon adhesions. The main question the clinical trial aims to answer is:\n\n\\- Can wrapping an amniotic membrane around a surgically released tendon help reduce recurrence of adhesions and promote recovery of hand functionality?\n\nParticipants will:\n\n* Undergo surgical treatment (surgical release of the tendon adhesions and wrapping of the amniotic membrane around the release tendon) on Day 0.\n* Visit the center for a series of tests 15 days, 6 weeks, 3 months, 6 months after the surgical intervention.",[25,26],"Tendon Adhesion","Tenolysis","RECRUITING","2024-12-04",{"date":30,"type":31},"2024-12-09","ACTUAL",{"date":33,"type":31},"2024-02-15",{"date":35,"type":19},"2026-08",{"name":37,"class":38},"TBF Genie Tissulaire","INDUSTRY",""]