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The study compares two treatment methods for improving pain and function in patients with de Quervain’s tenosynovitis

Phase 2
Conditions
Health Condition 1: M654- Radial styloid tenosynovitis [de Quervain]
Registration Number
CTRI/2024/08/072131
Lead Sponsor
Regional institute of medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Age between 20-60 years of both genders

2.Duration of symptoms less than 6 weeks

3.Visual analogue scale (VAS) = 4

4.Patients willing for study and follow up assessments.

Exclusion Criteria

1.Patients with uncontrolled diabetes

2.Congenital deformity of hand

3.Rheumatoid arthritis

4.Pregnancy

5.Local infection

6.Thrombocytopenia

7.Impaired cognition

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual analogue scale (VAS) <br/ ><br>Timepoint: <br/ ><br>1,4,12,24 weeks
Secondary Outcome Measures
NameTimeMethod
Quick DASHTimepoint: 1,4,12,24 weeks
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