Investigating the effect of percutaneous needle method in the repair of trigger finger

Not Applicable

• Conditions: Trigger finger.; Trigger finger; M65.3

• Registration Number: IRCT20230222057488N1
• Lead Sponsor: Iran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 March 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

People between 18 and 60 years old
Having a Trigger finger

Exclusion Criteria

Diabetic people
No previous reconstructive surgery

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The amount of release of A1 poly. Timepoint: Immediately after surgery. Method of measurement: Observation in open surgery method.

Secondary Outcome Measures

Name	Time	Method
Tendon damage. Timepoint: Immediately after surgery. Method of measurement: Observation in open surgery method.;Vascular damage. Timepoint: Immediately after surgery. Method of measurement: Observation in open surgery method.;Tissue damage. Timepoint: Immediately after surgery. Method of measurement: Observation in open surgery method.