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Effect of a traditional Iranian preparation in oligomenorrhea caused by polycystic ovary syndrome

Formulation and clinical trial of a traditional Iranian based preparation in oligomenorrhea caused by polycystic ovary syndrome (PCOS) in comparison with Dydrogesterone

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201610089618N3
Enrollment
120
Registered
2017-02-15
Start date
2016-08-20
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

polycystic ovary syndrome (PCOS). N95.1 Menopausal and female climacteric states

Interventions

Intervention 1: Intervention group: In this group 60 patients are provided with capsules containing traditional Iranian formulation. This patients are asked to fill the related forms regarding demogr
Treatment - Drugs
Intervention group: In this group 60 patients are provided with capsules containing traditional Iranian formulation. This patients are asked to fill the related forms regarding demographic informati
Control group: In this group 60 patients are provided with capsules containing dydrogesterone. This patients are asked to fill the related forms regarding demographic information and data about thei

Sponsors

Vice chancellor for research, Shiraz University of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Exclusion criteria: Pregnancy; lactation;abnormal prolactin level; abnormal thyroid hormone level; anatomical position which affects the study; sensitivity to herbal preparations. Inclusion criteria: single ladies; between 18 and 35 years of age; They have BMI between 20 and 30 and they are diagnosed with PCOS by Rotterdam criteria 2013.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Regular menstruation cycle. Timepoint: 2 cycles. Method of measurement: questionnaire.

Secondary

MeasureTime frame
BMI. Timepoint: Before the study and at the end of each mensturation cycle for 3 cycles. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAyda Hosseinkhani

Research center for traditional medicine and history of medicine

hoseinkhan@sums.a.cir+98 71132337589

Outcome results

None listed

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