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The effect of rehabilitation on patients with carpal tunnel syndrome after surgery

Phase 2
Conditions
Carpal Tunnel Syndrome.
Carpal Tunnel Syndrome
Registration Number
IRCT2017041233390N1
Lead Sponsor
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Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
30
Inclusion Criteria

Patients with carpal tunnel syndrome is diagnosed by a specialist and NCV test and Phalen tests and tinnel sign be positive; patients with idiopathic CTS; people who do not experience trauma and ankle injuries or have not had previous surgery.
Exclusion criteria: Injury or trauma during intervention; double Crush Syndrome; certain diseases such as rheumatoid arthritis, autoimmune and metabolic disorders

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Visual Analogue Scale.;Sensation. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Semmes Weinstein Test of Monofilaments.;Function. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Boston Questionnaire(function section).;Hand power(tip pinch, key pinch, grip). Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Vigorimeter.
Secondary Outcome Measures
NameTimeMethod
Symptoms. Timepoint: Befor surgery and intervention, 6 weeks after intervention and surgery and 8 weeks after intervention and surgery. Method of measurement: Boston Questionnaire(symptoms section).
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