Effect of Propolis capsule and Fennel capsule versus placebo on premenstrual syndrome

Effect of Propolis capsule and Fennel capsule versus placebo on premenstrual syndrome: a double-blind randomized clinical trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120215009014N525

Enrollment

Registered

2024-09-21

Start date

2024-10-06

Completion date

Unknown

Last updated

2025-01-08

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: Intervention group 1:Two 500 mg capsules of Propolis made by the Hamadan School of Pharmacy daily, 14 days before menstruation to 5 days after the onset of menstruation for two months.

Eligibility

Sex/Gender

Female

Age

18 Years to 25 Years

Inclusion criteria

Inclusion criteria: Age 18 to 25 years Being single Having regular periods with intervals of 21 to 35 days

Exclusion criteria

Exclusion criteria: Mental disorders and depression Amenorrhea or menstrual disorders

Design outcomes

Primary

Measure	Time frame
Signs and symptoms of premenstrual syndrome. Timepoint: Before the intervention and two months later. Method of measurement: By taking history and clinical examination.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArezoo Shayan

Hamedan University of Medical Sciences

arezoo.shayan2012@yahoo.com+98 81 3838 0572

Outcome results

None listed

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