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Clinical study for Drospirenone/Ethinyl Estradiol Tablet in the treatment of polycystic ovary syndrome

Clinical study for Drospirenone/Ethinyl Estradiol Tablet in the treatment of polycystic ovary syndrome

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022001
Enrollment
Unknown
Registered
2019-03-19
Start date
2017-10-01
Completion date
Unknown
Last updated
2019-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic ovary syndrome

Interventions

Case series:oral Drospirenone/Ethinyl Estradiol Tablet

Sponsors

Guangdong Women and Children Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
13 Years to 38 Years

Inclusion criteria

Inclusion criteria: Patients who qualified for PCOS as per the European Society of Human Reproduction and Embryology and the American Society of Reproductive Medicine at the Rotterdam Conference in 2003 were included. Additionally, patients with no contraindication to oral contraceptives, who were confident of being compliant to the drug and provided informed consent were also included.

Exclusion criteria

Exclusion criteria: Patients who are pregnant or lactating women;diagnosed with heart cerebrovascular, liver and kidney and hematopoietic system wait for serious primary disease, mental disease; diagnosed with malignant tumors, adrenal diseases or other diseases leading to organ failure;have used any hormone drugs or drugs affecting insulin secretion in the past 3 months;history of drug use for PCOS before inclusion in the study, and history of smoking and drug abuse; have poor compliance.

Design outcomes

Primary

MeasureTime frame
weight;Height;Waistline;Hipline;

Countries

China

Contacts

Public ContactLi Li

Guangdong Women and Children Hospital

13631446859@163.com+86 13631446859

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 28, 2026