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Effect of linseed oil in the treatment of carpal tunnel syndrome

Not Applicable
Conditions
Carpal tunnel syndrome.
Carpal tunnel syndrome
Registration Number
IRCT2012103111341N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Inclusion criteria: primary idiopathic carpal tunnel syndrome; patients aged between 18-65 years old; electrodiagnostic criteria for mild or moderate CTS; Patient's written informed consent for inclusion; having at least two signs or one sign plus one symptom of: paresthesias, numbness, tingling, night pain
positive Phalen test, positive Tinnel test, positive compression test.
Exclusion criteria: Clinical and electrodiagnostic evidence of severe CTS including muscular atrophy and neurogenic changes in needle EMG of APB muscle; recurrent carpal tunnel syndrome; Positive history of trauma and/or fracture of wrist bones and/or surgical release of median nerve and/or direct injection into carpal tunnel of wrist; Evidence of cervical radiculopathy in EMG; Systemic disease including: neuropathies (rule out by nerve conduction study of ulnar nerves) and/or collagen vascular diseases such as SLE and scleroderma and RA; Endocrine diseases such as hypothyroidism and DM; Other
disease-inducing neuropathy; Situations such as renal failure and/or alcoholism and/or poor medical condition; History of recent and ongoing use of corticosteroids or analgesics that could not be discontinued; hypersensitivity to the drug or placebo; inability to completion of data gathering forms (cognitive or language disorder).

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Median nerve wrist sensory nerve conduction velocity. Timepoint: beginning of the study and after 4 weeks. Method of measurement: electrodiagnosis.;Median nerve motor distal latency. Timepoint: beginning of the study and after 4 weeks. Method of measurement: electrodiagnosis.;Median nerve sensory distal latency. Timepoint: beginning of the study and after 4 weeks. Method of measurement: electrodiagnosis.;Median nerve compound latency. Timepoint: beginning of the study and after 4 weeks. Method of measurement: electrodiagnosis.;Boston Carpal Tunnel Questionnaire score. Timepoint: beginning of the study and after 4 weeks. Method of measurement: Boston Carpal Tunnel Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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