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Effect of vitamin d and vitamin e on premenstrual syndrome

Evaluating the Effects of vitamin d and vitamin e on the Severity of Premenstrual Syndrome in the affected persons that go to medical-health centers of isfahan university of medical sciences

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201401086854N2
Enrollment
150
Registered
2014-05-19
Start date
2011-09-23
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

Premenstrual syndrome. Premenstrual tension syndrome

Interventions

Intervention 1: Daily consumption of Vitamin D( Containing 200 mg of powdered vitamin D of MERK company, prepared by Isfahan Faculty of Pharmacy )or vitamin E(Containing 100 mg of powdered vitamin E o
Treatment - Drugs
Placebo
Daily consumption of Vitamin D( Containing 200 mg of powdered vitamin D of MERK company, prepared by Isfahan Faculty of Pharmacy )or vitamin E(Containing 100 mg of powdered vitamin E of MERK company,
Daily consumption of the placebo(Containing of Starch, prepared by Isfahan Faculty of Pharmacy) from the first day of the menstrual cycle until the first day of the next menstrual cycle for 2 cycles.

Sponsors

Vice chancellor for research,Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: being 15-45 years old; having regular menstrual cycle; not being affected by depression or anxiety; not having an acute or chronic disease; not taking medicines or supplements, and not taking regular exercise The exclusion criteria: pregnancy; willingness to use hormonal contraceptive methods or taking any hormonal treatment; not taking the drug or not filling out the forms regularly; and unwillingness to continue the treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Mean score of syndrome. Timepoint: 2 months before and 2 montha after. Method of measurement: Daily Rating Test.

Secondary

MeasureTime frame
Side effect. Timepoint: 2 months after intervention. Method of measurement: Questionaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Ebrahimi

Shahrood University Of MedicalSciences.

Ebrahimi_308@yahoo.com+98 21 7631 0158

Outcome results

None listed

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