MedPath

The effect of Primerose oil on Premenstrual syndrome

Not Applicable
Conditions
premenstural syndrome.
Premenstrual tension syndrome
Registration Number
IRCT201009214789N1
Lead Sponsor
Razi Herbal Drugs Research Center, Deputy of Research and Information Technology, Lorestan Universit
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
80
Inclusion Criteria

Age 18 - 35, having regular menstrual cycles with intervals 24 - 35 days , Without any physical diseases or specific drugs use, Analgesia drug for relieving pain , no record of mental diseases specially Depression disorder, no use of any anti depressants or hormonal drugs, no specific diet, no experience of stressful event during last 3 month from the beginning of the study and during the study
Exclusion criteria: Occurrence of the event during the study, having physical or mental diseases, pregnancy, lactation, menstrual cycle irregularity, medical diseases, using hormonal method of contraception

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intensity of the premenstrual syndrome. Timepoint: monthly during a period of 3 months. Method of measurement: The determination of total grade ( for any symptom from 0-10 ).
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath