Treatment of trigger finger
Phase 2
Completed
- Conditions
- Trigger finger.Trigger fingerM65.3
- Registration Number
- IRCT20180627040252N1
- Lead Sponsor
- Yazd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Age over 18 years
Patients with informed consent
Patients with trigger finger symptoms based on the QUINNELL scale.
Patients with no history of any previous finger surgery
Exclusion Criteria
Patients with hand tendon disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessing the finger movement. Timepoint: Weeks 1, 3 and 6 and then 3 and 6 months after intervention. Method of measurement: Physical examination.
- Secondary Outcome Measures
Name Time Method Pain after surgery. Timepoint: 1, 3 and 6 weeks and then 3 to 6 months after intervention. Method of measurement: Visual Analogue Scale (VAS).