A Comparative Study of the Different Dosages of Triamcinolone Acetonide in the Treatment of Trigger finger

Phase 4

Recruiting

• Conditions: trigger finger; trigger finger, steroid injection, triamcinolone acetonide, different doses

• Registration Number: TCTR20140914001
• Lead Sponsor: Mahavajiralongkorn Foundation

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-09-14
• Study Completion: 2015-05-11
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

trigger finger grade II - III

Exclusion Criteria

1. Patient who has the underlying such as DM, RA, OA of the fingers, gout and chronic renal disease.
2. Patient who has the history of trauma associated with the investigated finger.
3. Patient who has tenosynovitis of the investigated finger.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
recurrent rate 2 weeks, 1.5 month, 3 months, 6 months physical examination

Secondary Outcome Measures

Name	Time	Method
complications 2 weeks, 1.5 month, 3 months, 6 months physical examination