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Active Not RecruitingNCT07434999

Tendon Transfer for Correction of Pinch in Chronic Ulnar Nerve Injury

Evaluation of Combined ECRB and APL Tendon Transfer for Pinch Restoration in Chronic Ulnar Nerve Injury

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
17 (estimated)
Sponsor
Sohag University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This prospective study evaluates the outcomes of combined ECRB and APL tendon transfer for restoring pinch function in patients with chronic ulnar nerve injury. Patients will be followed postoperatively to assess improvement in hand function, strength, and daily activity performance. Participation is voluntary and all standard care procedures will be maintained

Detailed description

The study is a prospective, single-center interventional trial including adult patients diagnosed with chronic ulnar nerve injury affecting pinch function. Eligible participants will undergo combined ECRB (Extensor Carpi Radialis Brevis) tendon transfer to adductor pollicis tendon and APL (Abductor Pollicis Longus) tendon transfer to 1st dorsal interosseous tendon that performed by experienced surgeons. Preoperative evaluation includes baseline hand function, pinch strength, and disability assessment. Postoperative follow-up will occur at 4, 6, 12, and 24 weeks to measure functional improvement using standardized hand assessment tools. Adverse events will be monitored and recorded. Inclusion criteria: adults ≥18 years, chronic ulnar nerve injury \>6 months, and consent to participate. Exclusion criteria: prior tendon transfer, coexisting neuromuscular disorder, or inability to provide consent. Data will be anonymized to maintain confidentiality, and all ethical approvals will be in place.

Conditions

Interventions

TypeNameDescription
PROCEDURECombined ECRB and APL Tendon TransferThis surgical procedure involves transferring the Extensor Carpi Radialis Brevis (ECRB) and Abductor Pollicis Longus (APL) tendons to restore pinch function in patients with chronic ulnar nerve injury. Standard postoperative physiotherapy will follow, with assessments at 4, 6, and 12 weeks to monitor pinch strength, thumb mobility, and any complications

Timeline

Start date
2025-11-18
Primary completion
2025-12-20
Completion
2026-12-20
First posted
2026-02-27
Last updated
2026-02-27

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07434999. Inclusion in this directory is not an endorsement.