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Effect of vitamin D on quality of life in fibromyalgia pateints

Phase 3
Conditions
fibromyalgia syndrome.
Other soft tissue disorders, not elsewhere classified
Registration Number
IRCT2012100610960N2
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
45
Inclusion Criteria

20-70 years old females who fill ACR criteria 2010 of fibromyalgia and 25OHD level less than 30 ng/ml. Exclusions: rheumatologic disease; metabolic bone disease; diabetes; major depression; liver diseases; chronic kidney disease; cancer; malabsorption; pregnancy; steroid user; any extra-protocol vitamin D consumption; patients who had been treated with trazodon previously with no response.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Quality of life. Timepoint: On the day of recruitment ,4 and 8 weeks later. Method of measurement: SF36 and EQ-5D questionere.
Secondary Outcome Measures
NameTimeMethod
Rising of 25OH D level, comparison of sleep questioneer score before and after intervention in each group. Timepoint: on 1st day of recuitment, 4 and 8 weeks after intervention. Method of measurement: ELISA.
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