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Comparison of Acupuncture and Fluoxetine in the relief of pain in the patients with Fibromyalgia Syndrome (A clinical trial)

Not Applicable
Conditions
Fibromyalgia.
Fibromyalgia
Registration Number
IRCT138902013767N1
Lead Sponsor
Shiraz Univesity Of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Inclusion Criteria: history of the presence of at least 3 months of widespread pain that is bilateral, on the both above and below the waist, pain on palpation of at least 11 of 18 predefined tender points

Exclusion Criteria

abnormal lab data, night employment

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Baseline and 2, 4, and 8 weeks after intervention. Method of measurement: VAS & FIQ.
Secondary Outcome Measures
NameTimeMethod
Fibromyalgia signs and symptoms. Timepoint: Baseline and 2, 4, and 8 weeks after intervention. Method of measurement: via VAS & FIQ questionnaire.
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