Efficacy of Intraoperative autologous platelet rich plasma injection during carpal tunnel release. A double-blind, randomized controlled trial
- Conditions
- Moderate to severe carpal tunnel syndrome patients requiring carpal tunnel release surgerycarpal tunnel syndromesevere carpal tunnel syndromecarpal tunnel releaseplatelet-rich plasmaPRP
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 35
1. Age more than 18 years old
2. Diagnosed with carpal tunnel syndrome using criteria of 2/2 1. Pain or numbness at thumb index middle and radial half of ring finger 2. a positive physical examination of Tinel's sign or Phalen test, or Durkan test
3. Electrodiagnostic confirmed with moderate to severe carpal tunnel syndrome according to American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) guideline
4. Persist symptoms at least 3 months after conservative treatment and requiring carpal tunnel release surgery
1. Previous PRP or steroid injection in 6 months
2. History of Inflammatory joint disease e.g. RA, SLE, gouty arthritis
3. History of Peripheral neuropathy, Cervical spondylosis radiculopathy
4. Previous fracture/injury or surgery on the affected hand
5. Cognitive impairment
6. History of Thrombocytopenia or Thrombocytosis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Thai version BCTQ 3 month Thai version boston carpal tunnel questionaire (BCTQ)
- Secondary Outcome Measures
Name Time Method