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The effect of Primerose oil on Premenstrual syndrome

The effect of Primerose oil on Premenstrual syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201009214789N1
Enrollment
80
Registered
2010-12-01
Start date
2010-10-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

premenstural syndrome. Premenstrual tension syndrome

Interventions

Intervention 1: Primerose oil capsule, 1500 mg/day (500 mg, TDS ) for 12 weeks. Intervention 2: Placebo capsule (TDS) for 12 weeks.
Treatment - Drugs
Placebo
Primerose oil capsule, 1500 mg/day (500 mg, TDS ) for 12 weeks
Placebo capsule (TDS) for 12 weeks

Sponsors

Razi Herbal Drugs Research Center, Deputy of Research and Information Technology, Lorestan Universit
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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 ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMandana Saki

Lorestan University of Medical Sciences

saki.m@lums.ac.ir , mandana_saki@yahoo.com+98 66 1620 0140

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026