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Effect of self-stretching on the clinical and electrophysiology symptoms of patients with carpal tunnel syndrome

Phase 3
Recruiting
Conditions
G56.0
Carpal tunnel syndrome.
Carpal tunnel syndrome
Registration Number
IRCT20120215009014N511
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
96
Inclusion Criteria

Age 18 to 90 years
Carpal tunnel syndrome

Exclusion Criteria

Neuropathic disorders
History of surgery or trauma to the wrist

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Average pain intensity. Timepoint: Before the intervention and 6 weeks later. Method of measurement: Using the visual analog scale (VAS).;Sensory disorder of the fingers. Timepoint: Before the intervention and 6 weeks later. Method of measurement: Using nerve and muscle tape.;Amplitude and sensory and motor latency of the median nerve. Timepoint: Before intervention and 6 weeks later. Method of measurement: Using nerve and muscle tape.;Clinical symptoms. Timepoint: Before the intervention and 6 weeks later. Method of measurement: Using the Boston Clinical Criteria.
Secondary Outcome Measures
NameTimeMethod
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