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Comparison of combined oral contraceptive Yasmin and Cyproteron compound on Hirsutism and androgens in women with a polycystic ovary syndrome

Comparison of combined oral contraceptive Yasmin and Cyproteron compound on Hirsutism and androgens in women with a polycystic ovary syndrome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104251760N13
Enrollment
100
Registered
2012-03-04
Start date
2012-02-20
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

Condition 1: Polycystic ovarian syndrome. Condition 2: Hirsutism. Polycystic ovarian syndrome Hypertrichosis

Interventions

Intervention 1: Intervention Groups: Yasmin pills (containing Drospirenone 3 mg+30 g Ethinyl Estradiol), from 1-21 day cycle for 4 months. Intervention 2: Control group: Cyproterone Compound Tablets (
Treatment - Drugs
Intervention Groups: Yasmin pills (containing Drospirenone 3 mg+30 g Ethinyl Estradiol), from 1-21 day cycle for 4 months.
Control group: Cyproterone Compound Tablets (2 mg Cyproteron acetate + 35 µg Ethinyl Estradiol) from day 21 to 1 cycle for 4 months.

Sponsors

Vice Chancellor for Research and Technology, Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 28 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 18-28 years old nonsmoker women with polycystic ovary syndrome and Hirsutism who are raftered to our research center for treatment of Hirsutism and taking contraceptive necessities. Exclusion criteria: Hyper-prolactinemia; Hypothyroidism; diabetes; doing regular intense exercise; taking diet or herbal treatment, Non-steroidal anti- inflammatory drugs, diuretics, or hormone therapy during last 3 months.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Back spontaneous menstrual. Timepoint: 6 months after cessation of treatment. Method of measurement: Clinical examination.

Secondary

MeasureTime frame
Side effects of drugs (such as complaints of headaches and spotting). Timepoint: 4 months. Method of measurement: Clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Molod Aghajani-delavar

Fatemehzahra Infertility & reproductive Health Research Center

moloodaghajani@yahoo.com+98 11 1227 4881

Outcome results

None listed

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