Status:
TERMINATED
Flexor Tenosynovectomy to Treat Recurrent Carpal Tunnel Syndrome
Lead Sponsor:
University of Tennessee
Conditions:
Carpal Tunnel Syndrome
Eligibility:
All Genders
18+ years
Brief Summary
The purpose of this study is to collect data on the clinical and functional outcomes of surgical management for recurrent carpal tunnel syndrome (CTS) using flexor tenosynovectomy. It is hypothesized ...
Detailed Description
Primary carpal tunnel release (CTR) is the most common surgical procedure of the hand, but reported rates of symptom recurrence are not uncommon. Many surgical techniques have been proposed and report...
Eligibility Criteria
Inclusion
- Adult patients (\> 18 years)
- Patient of The Plastic Surgery Group/Hayes Hand Center
- Previous diagnosis of Carpal Tunnel Syndrome
- Diagnosis of Recurrent Carpal Tunnel Syndrome
- Underwent primary carpal tunnel release
- Undergoing isolated flexor tenosynovectomy as secondary procedure
Exclusion
- Had incomplete primary release of transverse carpal ligament
- Had documented neuroma upon re-exploration
- Had other soft tissue tumor within carpal tunnel or providing reasonable contribution to neurologic symptoms
- Experienced fracture or other traumatic injury to wrist after primary carpal tunnel release
- Diagnosis of osteomyelitis, infectious tenosynovitis or other infectious etiology to area of interest after primary procedure
- Diagnosis of rheumatoid arthritis, psoriatic arthritis, or other inflammatory arthropathy
Key Trial Info
Start Date :
February 1 2016
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
November 1 2018
Estimated Enrollment :
2 Patients enrolled
Trial Details
Trial ID
NCT03757416
Start Date
February 1 2016
End Date
November 1 2018
Last Update
November 28 2018
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