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Comparison of the effect of Primerose oil and Vitamin B6 versus placebo on premenstrual syndrome in girl college students

Phase 2
Conditions
premenstrual syndrome.
Premenstrual tension syndrome
Registration Number
IRCT201610289014N127
Lead Sponsor
Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

age of 18 to 35 years; having regular menstrual cycle with 21 to 35 days interval.
Exclusion criteria: physical disease or using medications; psychological disease; using anti-depression drugs during past months; using hormonal drugs or vitamins.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of symptoms of premenstrual syndrome. Timepoint: before intervention and 1 and 2 months after intervention. Method of measurement: using standard diagnostic questionnaire for premenstrual syndrome.
Secondary Outcome Measures
NameTimeMethod
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