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Evaluation of the effectiveness of TECAR therapy in carpal tunnel syndrome

Not Applicable
Recruiting
Conditions
Carpal tunnel syndrome.
Carpal tunnel syndrome
G56.0
Registration Number
IRCT20220405054422N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

Patient with unilateral or bilateral idiopathic mild and moderate carpal tunnel syndrome confirmed by EMG-NCS and clinical test and lasting more than one month.

Exclusion Criteria

Systemic and local diseases (diabetes, RA, wrist arthritis, hypothyroidism, etc.)
Cancer
Pregnancy
Burns on the hands and forearms
IUD, Pacemaker, prosthesis
Peripheral vascular diseases
Fractures in the wrist and hand area
Corticosteroid injection in the last trimester in the carpal tunnel

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Symptom severity scale. Timepoint: At the beginning of the study and 1 and 2 months after treatment. Method of measurement: Boston Carpal Tunnel Syndrome Questionnaire.;Functional status. Timepoint: At the beginning of the study and 1 and 2 months after treatment. Method of measurement: Boston Carpal Tunnel Syndrome Questionnaire.;Pain. Timepoint: At the beginning of the study and 1 and 2 months after treatment. Method of measurement: Visual Analogue Scale.;Median SNAP peak latency. Timepoint: At the beginning of the study and 2 months after treatment. Method of measurement: EMG machine.;Median motor onset latency. Timepoint: At the beginning of the study and 2 months after treatment. Method of measurement: EMG machine.;Median SNAP amplitude. Timepoint: At the beginning of the study and 2 months after treatment. Method of measurement: EMG machine.;Median sensory NCV across wrist. Timepoint: At the beginning of the study and 2 months after treatment. Method of measurement: EMG machine.
Secondary Outcome Measures
NameTimeMethod
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