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The ovulation-induced therapy for polycystic ovary syndrome

The ovulation-induced therapy for polycystic ovary syndrome

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001821
Enrollment
Unknown
Registered
2011-12-12
Start date
2011-10-01
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 ovary syndrome

Interventions

A:5mg letrozole qd from the 3rd day of menstruation
B:50~150mg clomiphene qd from the 3rd day of menstruation for 5 days
C:500mg metformin tid immediately and 50~150mg clomiphene qd from the 3rd day of menstruation for 5 days.Medication was discontinued when pregnancy was confirmed.
D:500mg metformin tid immediately and 5mg letrozole qd from the 3rd day of menstruation for 5 days.Medication was discontinued when pregnancy was confirmed.

Sponsors

West China Women's and Children's Hospital S.C.U
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are diagnosised as PCOS based on the Revised 2003 consensus diagnostic criteria for PCOS; 2. The PCOS patients who want to give birth to a baby; 3. patients With clinical and/or biochemical signs of hyperandrogenism and/or insulin resistance.And those patients need to receive a 3-6 months anti-androgen and/or anti-insulin therapy before included in until above symptons have been relieved.

Exclusion criteria

Exclusion criteria: 1. with other factors affecting pregnance; (1) dysfunction of ovarian ducts:hydrosalpinx,obstruction,stenosis; (2) uterine abnormalities,such as submucous myoma in submucosa or cornua,uterine malformation,intrauterine adhesions,chocolate cyst; (3) abnormal serum PRL or thyroidal disfunction; (4) a positive pulmonary or pelvic TB history; (5) abnormal semen; 2. clinical and/or biochemical signs of hyperandrogenism; 3. BMI>30kg/m2; 4. age>35 years old.

Design outcomes

Primary

MeasureTime frame
ovulation rate;pregnancy rate;live birth rat;

Secondary

MeasureTime frame
pregnancy lost rate;multipregnancy rate;OHSS morbidity;

Countries

China

Contacts

Public ContactWei Huang
weihuang64@163.com+86 028 85501073

Outcome results

None listed

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