[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"flexor-tendon\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:flexor-tendon":67},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":27,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":4},"100622328",false,"NCT07382193","Evaluation of Eight-Strand Flexor Tendon Repair Without Splinting","Evaluation of the Eight - Strand Repair of Flexor Tendon Injuries Without Splinting a Prospective Cohort Study","Inclusion Criteria:\n\n* Adult patients (18+ years).\n* Single or multiple clean-cut flexor tendon injuries.\n* Primary repair performed within 2 weeks.\n* Patients with concurrent digital nerve injuries will include if the nerve could be directly repaired.\n\nExclusion Criteria:\n\n* Crush or avulsion injuries.\n* Associated fractures or neurovascular compromise.\n* Recurrent or chronic tendon injuries.","ALL","18 Years",{"count":18,"type":19},40,"ESTIMATED","OBSERVATIONAL","This prospective cohort study evaluates functional outcomes of primary eight-strand flexor tendon repair in zone II without postoperative splinting in 40 adults (≥18 years) at Assiut University Hospitals. Patients undergo wide-awake local anesthesia no tourniquet (WALANT) surgery followed by immediate gentle active motion. Primary outcome: total active motion via Strickland score at 6 weeks and 6 months. Secondary: grip strength, DASH score, patient satisfaction.",[23,24,25,26],"Flexor Tendon Injury","Splints","Flexor Tendon Repair","Flexor Tendon",[28,29,30],"Eight-strand repair","Flexor tendon injury","no splint","NOT_YET_RECRUITING","2026-01-26",{"date":34,"type":35},"2026-02-02","ACTUAL",{"date":37,"type":19},"2026-03",{"date":39,"type":19},"2027-04",{"name":41,"class":42},"Assiut University","OTHER",{"id":44,"slug":4,"hasResults":10,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":48,"enrollmentInfo":49,"targetDuration":4,"studyType":51,"phases":52,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":66},"100387256","NCT04322370","Prospective Randomized Blinded Trial of VersaWrap Tendon Protector for Zone 2 Flexor Tendon Injuries","Inclusion Criteria:\n\n* Adult patients presenting to the plastic surgery service with a zone 2 flexor tendon injury requiring surgical repair\n\nExclusion Criteria:\n\n* Patients with a sensitivity or allergy to polysaccharides alginate, hyaluronic acid, or citrate\n\n  * Patients with psychiatric or medical problems that preclude them from having surgery\n  * Female patients that are pregnant or breastfeeding\n  * Prisoners\n  * Patients who are unwilling or unable to follow-up","99 Years",{"count":50,"type":19},42,"INTERVENTIONAL",[53],"NA","To analyze outcomes between patients with Z2FT injuries following repair, randomized to two groups. The first group will be the negative control, with no tendon wrap. The second group will have a VersaWrap Tendon Protector applied over the site of the tendon repair. VersaWrap is current SOC at UF.",[26],"RECRUITING","2025-03-12",{"date":59,"type":35},"2025-03-17",{"date":61,"type":35},"2020-08-21",{"date":63,"type":19},"2027-05-17",{"name":65,"class":42},"University of Florida",1,""]