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Comparison of Piperine, Vitamin E, and Piperine with Vitamin E Oral Capsules Effects on Premenstrual Syndrome

Comparison of Piperine, Vitamin E, and Piperine with Vitamin E Oral Capsules Effects on Premenstrual Syndrome among Dormitory Students

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201508022172N19
Enrollment
180
Registered
2016-01-04
Start date
2016-01-05
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 (PMS). Premenstrual tension syndrome

Interventions

Intervention 1: Taking two oral capsules in a day (capsule with 8 mg Piperine, and capsule with 50 mg Gelatin) for two weeks in 2 months intervention. Intervention 2: Taking two oral capsules in a day
Treatment - Drugs
Placebo
Taking two oral capsules in a day (capsule with 8 mg Piperine, and capsule with 50 mg Gelatin) for two weeks in 2 months intervention
Taking two oral capsules in a day (capsule with 8 mg Piperine, and capsule with 400 IU vitamin E) for two weeks in 2 months intervention
Taking two oral capsules in a day (capsule with 400 IU vitamin E, and capsule with 50 mg Gelatin) for two weeks in 2 months intervention
Taking two oral capsules of 50 mg Gelatin in a day for two weeks in 2 months intervention

Sponsors

Vice chancellor for research and technology, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 18 and 35 years old; being single; being healthy regarding to their self-report and physical examination; having regular menstrual cycles (22-35 days and 2-7 days duration); having premenstrual syndrome (PMS) in 2 past cycles (no sever syndrome); no history of allergy to any food; not taking any medicine; not taking any complements; not smoking, alcohol or drug usage; no history of pregnancy. Exclusion criteria: use of any kind of drug or therapy for symptom relief during the study intervention; side effects during intervention for example allergy; change in diet or physical exercise program during the study; any kind of crisis in participant or her family; not taking capsules more than 7 days in 2 cycles

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Premenstrual syndrome (screening). Timepoint: 2 menstrual cycles. Method of measurement: premenstrual profile 2005 scale.

Secondary

MeasureTime frame
Premenstrual syndrome (prevention). Timepoint: During intervention for 2 cycles. Method of measurement: Measure by premenstrual profile 2005 scale, for duration of 2 cycles.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSimin Taavoni

Iran University of Medical Sciences

staavoni14@yahoo.com+98 21 6692 1228

Outcome results

None listed

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