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Clinical and Metabolic Effects of Rosiglitazone on Women with Polycystic Ovarian Syndrome

Clinical and Metabolic Effects of Rosiglitazone on Women with Polycystic Ovarian Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-09000670
Enrollment
Unknown
Registered
2005-11-14
Start date
2004-11-18
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Polycystic Ovarian Syndrome

Interventions

Two groups:Rosiglitazone 4mg B.D. (8mg per day) 12 months versus Placebo 1 tab B.D.

Sponsors

None listed

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: INCLUSION CRITERIA: (At least 2 of the major criteria listed below) Major criteria: 1. Anovulation (with other causes of anovulation excluded); 2) Clinical signs of hyperandrogenism (hirsutism or acne) and/or hyperandrogenemia (with other causes of hyperandrogenemia excluded); Minor criteria: 1) Elevated early follicular phase (LH >10 IU/L); 2. Elevated LH/FSH ratio >2.5); 3. Polycystic ovaries on ultrasound scan; 4. Obesity (BMI > 25) / Insulin resistance.

Exclusion criteria

Exclusion criteria: EXCLUSION CRITERIA: 1. Women with PCOS who are planning for pregnancy, or undergoing fertility treatment; 2. Women with PCOS who are already on oral hypoglycaemic agents or insulin treatment; 3. Women with cardiovascular disease, hepatic or renal function impairment; 4. Women on corticosteroid therapy; 5. Women with known endometrial hyperplasia.

Design outcomes

Primary

MeasureTime frame
Menstrual status; hirsutism score, free testosterone, SHBG level;

Secondary

MeasureTime frame
IMT (Intima Madia Thickness);

Countries

China

Contacts

Public ContactProf. Tam Wing Hung
tamwh@cuhk.edu.hk+852 2632 2802

Outcome results

None listed

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