Skip to content

A multicenter, randomised controlled trials on the effect of antiandrogenic pretreatment on assisted reproductive technology outcomes in non-obese PCOS patients with hyperandrogenism

A multicenter, randomised controlled trials on the effect of antiandrogenic pretreatment on assisted reproductive technology outcomes in non-obese PCOS patients with hyperandrogenism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073122
Enrollment
Unknown
Registered
2023-07-03
Start date
2023-07-03
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

PCOS

Interventions

OC preconditioning group:After using OC(yasmin) to resist androgen for 3 cycles before entering the ovulation induction cycle
control group:entering the ovulation induction cycle directly without resist androgen

Sponsors

Women's Hospital School of Medicine Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1) Age: 20-40 years old, accepting IVF/ICSI for pregnancy; 2) 18.5Kg/m2=BMI<24Kg/m2 3) Patients with polycystic ovary syndrome following hyperandrogens; 4) Currently or in the past 3 months, have not participated in other research projects; 5) Sign informed consent form;

Exclusion criteria

Exclusion criteria: 1) Other endocrine diseases accompanied by hyperandrogenism, such as Cushing's syndrome, congenital adrenal hyperplasia, ovarian or adrenal tumors, as well as other inflammatory diseases, autoimmune diseases, malignant tumors (such as Crohn's disease, ulcerative colitis, rheumatoid arthritis, systemic lupus erythematosus, hypertension, benign or malignant hematological diseases, etc.); 2) Other endocrine diseases such as neurological and psychiatric diseases, coronary heart disease, adrenal diseases, thrombotic diseases, pituitary microadenoma, thyroid dysfunction, etc.; 3) Ovarian cysts, uterine fibroids (diameter =4cm), adenomyosis, severe hydrosalpinx, severe endometriosis (stage III-IV); 4) History of ovarian or uterine tumor surgery and other major organ surgeries; 5) Severe intrauterine adhesions; 6) Oral contraceptives, glucocorticoids, immunosuppressants, antihypertensive drugs, lipid-lowering drugs, and other anti-androgenic drugs taken within the past 3 months; 7) Testicular biopsy for sperm retrieval for ICSI; 8) Smokers and alcohol drinkers; 9) Contraindications to oral contraceptives; 10) Other situations deemed inappropriate by the researcher and unable to participate in follow-up

Design outcomes

Primary

MeasureTime frame
Reproductive hormone tests;BUS;Pregnancy-related indicators;

Secondary

MeasureTime frame
Complete blood count;Coagulation function;Thyroid function;Liver and kidney function;Blood lipid test;OGTT-IRT;

Countries

China

Contacts

Public ContactGuofang Feng

Women's Hospital School of Medicine Zhejiang University

fbfgf@zju.edu.cn+86 138 1945 1219

Outcome results

None listed

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