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Study on the research of serum AMH cutoff value in patients with polycystic ovary syndrome in China

Study on the research of serum AMH cutoff value in patients with polycystic ovary syndrome in China

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027842
Enrollment
Unknown
Registered
2019-11-30
Start date
2019-11-25
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

Polycystic ovary syndrome

Interventions

Gold Standard:1. Sparse ovulation or anovulation
2. Clinical manifestations of high androgen and hyperandrogenism
3. Polycystic ovaries visualized through ultrasonography: one or both sides of the ovary with a diameter of 2-9 mm follicles >= 12 and / or ovarian volume >= 10 cm3. Two of the above three articles we
Index test:Elecsys AMH

Sponsors

Beijing Obstetrics & Gynecology Hospital,Capital Medical university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 20-40 years old women of childbearing age 1. PCOS group: (1) Sparse ovulation or anovulation; (2) Clinical manifestations of high androgen and hyperandrogenism; (3) Polycystic ovaries visualized through ultrasonography: one or both sides of the ovary with a diameter of 2-9 mm follicles >= 12 and / or ovarian volume >= 10 cm3. Two of the above three articles were excluded, and other diseases causing hyperandrogen such as congenital adrenal hyperplasia and Cushing syndrome were excluded. It can be diagnosed as PCOS. 2. Normal control group: (1) Women who have been examined before pregnancy; (2) Regular menstruation, no history of PCOS.

Exclusion criteria

Exclusion criteria: (1) Currently treated with sex hormones within 3 months prior to enrollment (long-acting treatment for 6 months); (2) There are diseases related to coagulopathy; (3) Cushing's syndrome; (4) Functional uterine bleeding; (5) hypothalamic-pituitary amenorrhea; (6) hyperprolactinemia; (7) premature ovarian failure; (8) ovarian functional tumors; (9) ovarianhyperthecosis; (10) Other patients identified by the investigator as unsuitable for participation in the study; (11) Known or suspected pregnancy.

Design outcomes

Primary

MeasureTime frame
anti-Mullerian hormone;

Countries

China

Contacts

Public ContactXiangyan Ruan

Beijing Obstetrics & Gynecology Hospital, Capital Medical university

ruanxiangyan@163.com+86 13011215678

Outcome results

None listed

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