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Key hole surgery for carpal tunnel syndrome

Not Applicable
Conditions
Health Condition 1: null- Carpal Tunnel Syndrome
Registration Number
CTRI/2012/05/002693
Lead Sponsor
Goa Medical College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
52
Inclusion Criteria

Patient of both gender and are more than or equal to 18 years of age

Patient provided signed/dated Informed Consent after receiving a full explanation of the extent and nature of the study.

Patient with Carpal Tunnel Syndrome which is defined by presence of clinical findings (e.g., symptoms of numbness, tingling, or burning pain of the hand, and decreased sensation to pin in palm and first 3 digits) and is confirmed by Electromyography (NICE guidelines & Guidelines by AAOS)(3, 6)

Exclusion Criteria

Pregnant or breast feeding women

Rheumatiod arthritis

Previous fractures around the wrist

Previously operated for release of Carpal Tunnel

Participation in a clinical trial within 1 month prior to study start

Patient with Gout, amyloid diseae

Patient with tumour causing Carpal Tunnel Syndrome, for example ganglion

Patients with isolated motor branch compression of median nerve.

Peripheral neuropathy

Localised infection of the hand and oedema of the hand

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess for the improvement in CTS by using Boston Carpal Tunnel Syndrome Questionnaire at the end of 3 months post operativelyTimepoint: End of 3 months post operatively
Secondary Outcome Measures
NameTimeMethod
ï?§Incidence of serious and non-serious adverse events and nature of adverse event post operatively <br/ ><br>ï?§To assess the improvement in CTS using electromyography <br/ ><br>ï?§Assessment of return to full activity which will be determined at visit 3, 4 and 5 <br/ ><br>ï?§Assessment of grip strength <br/ ><br>Timepoint: at the end of 3 months post operatively
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