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Study of the effect of wrist mobilization on carpal tunnel syndrome

Phase 3
Conditions
carpal tunnel syndrome.
Carpal tunnel syndrome, unspecified upper limb
G56.00
Registration Number
IRCT20180511039611N1
Lead Sponsor
Artesh University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
52
Inclusion Criteria

Carpal tunnel syndrome approved by electrodiagnostic criteria
Age 30 to 60 years old and with any sex

Exclusion Criteria

Atrophy of tenar muscle, mild or severe CTS based on electrodiagnostic study
patient who was treated with anti-inflammatory drugs or physiotherapy modalities
previous local steroids injection in a recent year or previous surgery for CTS
Inflammatory joint disease, diabetes mellitus, thyroid disease
Polyneuropathy, cervical radiculopathy, myelopathy
Pregnancy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Electrodiagnostic parameters of Median nerve (sensory and motor latency and amplitude). Timepoint: Before and two months after treatment. Method of measurement: By electrodiagnostic device (Medtronic Dk-2740 denmark).
Secondary Outcome Measures
NameTimeMethod
Pain intensity. Timepoint: Before, one and two months after treatment. Method of measurement: By visual analogue scale.;Symptom severity and functional status. Timepoint: Before, one and two months after treatment. Method of measurement: By Boston carpal tunnel questionnaire.;Patient satisfaction. Timepoint: 6 months after treatment. Method of measurement: By telephone.
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