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Comparison of the effects of combined use of recombinant follicle stimulating hormone and letrozole with follicle stimulating hormone alone on single live birth rate in patients with polycystic ovary syndrome

Comparison of the effects of combined use of recombinant follicle stimulating hormone and letrozole with follicle stimulating hormone alone on single live birth rate in patients with polycystic ovary syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035117
Enrollment
Unknown
Registered
2020-08-01
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-03

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

Conditions

polycystic ovary syndrome

Interventions

Group A:Letrozole will be taken on the 3rd to 7th day of menstrual cycle, recombinant follicle stimulating hormone will be injected on the 7th to 11th day
Group B:Recombinant follicle stimulating hormone will be injected from the 3rd day of the menstrual cycle, the frequency and dosage will be adjusted according to the growth of follicles

Sponsors

The Third Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 42 Years

Inclusion criteria

Inclusion criteria: 1. Patients with PCOS who wish to conceive. The diagnostic criteria for PCOS are as follows (Rotterdam criteria): (1) oligoovulation or anovulation; (2) clinical manifestations of hyperandrogen and/or hyperandrogenemia; (3) ovarian polycystic changes. 2. Aged 18-42 years. 3. At least one unobstructed fallopian tube and normal uterine cavity. 4. Willing to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications to assisted reproductive technology or pregnancy contraindications: such as uncontrolled diabetes, uncontrolled hypertension, heart disease, endometrial cancer, breast cancer, and unclearly diagnosed vaginal bleeding. 2. All male factors leading to infertility. 3. Urine and/or blood human chorionic gonadotropin test positive. 4. History of pregnancy (abortion or childbirth) within 12 months. 5. Abnormal uterine cavity. 6. History of repeated miscarriages. 7. Moderate or severe endometriosis. 8. Moderate or severe hydrosalpinx. 9. One of the husband and wife has abnormal chromosomes.

Design outcomes

Primary

MeasureTime frame
cumulative single live birth rate;

Secondary

MeasureTime frame
clinical pregnancy rate;miscarriage rate;multiple pregnancy rate;ongoing pregnancy rate;cycle cancellation rate;single follicle rate;rate of OHSS;

Countries

China

Contacts

Public ContactYichun Guan

The Third Affiliated Hospital of Zhengzhou University

lisamayguan@126.com+86 13608695579

Outcome results

None listed

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