Effect of tenosynovectomy on de Quervain's decompression surgery: a randomized controlled trial
Phase 3
Recruiting
- Conditions
- de Quervain's tenosynovitiss tenosynovitis, tenosynovectomy, functional outcome
- Registration Number
- TCTR20221124001
- Lead Sponsor
- /A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 106
Inclusion Criteria
1. first time first extensor compartment decompression
Exclusion Criteria
1. Recurrent de Quervain's tenosynovitis after surgery, 2. simultaneous surgical treatment of other diseases of hand, 3. pregnancy or lactation, 4. allergy to lidocaine, bupivacaine, paracetamol, and NSAIDs, 5. Poor understanding of protocal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain 1 month Numerical rating scale
- Secondary Outcome Measures
Name Time Method Pain within 3 months numerical rating scale,Analegic drug use within 3 months Pill count measure,Hand and wrist function within 3 months patient-rated wrist evaluation (PRWE),Hand and wrist function within 3 months Quick Disabilities of the arm, shoulder, and hand (QuickDASH),Quality of life within 3 months EQ-5D-5L,Pinch strength within 3 months Pinch gauge,Complication within 3 months Physical examination