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Establishment of standardized ovulation induction protocol for patients with polycystic ovary syndrome-related infertility

Establishment of standardized ovulation induction protocol for patients with polycystic ovary syndrome-related infertility

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031270
Enrollment
Unknown
Registered
2020-03-26
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-03-30

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 1:Letrozole, one tablet each day, 5 days
Group 2:Clomiphene citrate, one tablet each day, 5 days
Group 3:Letrozole, one tablet each day, and Clomiphene citrate, one tablet each day, 5 days.

Sponsors

The First Affiliated Hospital of University of South China
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Infertile patients with PCOS; 2. Patients aged 18-35; 3. BMI 18.5-28.

Exclusion criteria

Exclusion criteria: 1. Infertile patients with other fallopian tube factors; 2. Those who are infertile due to male factors; 3. With endometriosis or other ovulation disorder.

Design outcomes

Primary

MeasureTime frame
Single follicle ovulation rate = single dominant follicle development and ovulation/induction cycle;—

Secondary

MeasureTime frame
Biochemical pregnancy rate;Clinical pregnancy rate;Live birth rate;—

Countries

China

Contacts

Public ContactOuyang Shuming

The First Affiliated Hospital of University of South China

ouyang-008@163.com+86 13973469180

Outcome results

None listed

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