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Effects of needling on the reduction of upper limb's pai

Phase 2
Conditions
Carpal tunnel syndrome.
Carpal tunnel syndrome
Registration Number
IRCT201602051292N4
Lead Sponsor
Vice chancellor for research, Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

having mild to moderate CTS; willingness to participate in the study.
Exclusion criteria: any history of local injection or surgery related to CTS; radiculopathy; coexisting disease (rheumatoid arthritis, osteoarthritis, diabetes, and hypothyroidism); severe CTS.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patients' pain. Timepoint: Before, one and sex weeks after intervention. Method of measurement: Using visual analogue scale.
Secondary Outcome Measures
NameTimeMethod
Patient' functional status. Timepoint: Before, one and six weeks after intervention. Method of measurement: Using Boston questionnare.
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