Evaluation of the effect of interventions near and far to the carpal tunnel using dry needle method and routine physiotherapy

Phase 2

Recruiting

• Conditions: Carpal tunnel syndrome.; Carpal tunnel syndrome; G56.0

• Registration Number: IRCT20130612013651N4
• Lead Sponsor: Vice Chancellor for Research, Yazd University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 August 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

Having clinical signs to diagnose carpal tunnel syndrome.
Have symptoms of the disease in the last 6 months.
Age range 20 to 65 years.

Exclusion Criteria

Pregnancy.
Having a history of carpal tunnel syndrome hand surgery.
systemic diseases.
Therapeutic intervention has been performed in the last 6 months.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Median nerve conduction velocity. Timepoint: Before and after the intervention and one month follow-up interval. Method of measurement: electromyography device.;Muscle and fascia thickness. Timepoint: Before and after the intervention and follow-up interval. Method of measurement: sonography.

Secondary Outcome Measures

Name	Time	Method
Pain intensity. Timepoint: Before and after the intervention and follow-up interval. Method of measurement: Visual analoug scale.;Functional ability. Timepoint: Before and after the intervention and follow-up interval. Method of measurement: Boston Questionnaire.