Evaluation of the effectiveness of metacarpophalengeal static splint on the adult patients with trigger finger

Not Applicable

• Conditions: The adult patients with trigger finger.; Trigger finger; M65.3

• Registration Number: IRCT20180804040685N3
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 August 2021

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

20-80 y/o
The individuals should not have received similar treatments before and during this study
One affected finger
No contraindication for injection
All participants should receive and fill the consent form
No contraindication for splinting
SST>2

Exclusion Criteria

The patients with CNS disorder, peripheral neuropathy and osteoarthritis
Who has proper cooperation in the course of study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Functional status. Timepoint: Beginning of the study (before intervention), one month and three months after intervention. Method of measurement: Boston assessment questionnaire.;Pain. Timepoint: Beginning of the study (before intervention), one month and three months after intervention. Method of measurement: Numeric pain rating.;The strength of the fingers. Timepoint: Beginning of the study (before intervention), one month and three months after intervention. Method of measurement: Dynamometer.;Stage of disease. Timepoint: Beginning of the study (before intervention), one month and three months after intervention. Method of measurement: Stages of stenosing tenosynovtits.