Evaluation of Eight-Strand Flexor Tendon Repair Without Splinting

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.

NCT Number	NCT07382193
Lead Sponsor	Assiut University
Conditions	Flexor Tendon Injury, Splints, Flexor Tendon Repair, Flexor Tendon
Enrollment	40 participants
Start Date	2026-03
Primary Completion	2027-03 (estimated)
Study Completion	2027-04 (estimated)
Updated on ClinicalTrials.gov	2026-02-02