FindTrial
Sign In

Multi-center Clinical Study on Premature Ovarian Insufficiency (POI) in China

Multi-center Clinical Study on Premature Ovarian Insufficiency (POI) in China

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000040611
Enrollment
Unknown
Registered
2020-12-03
Start date
2021-01-07
Completion date
Unknown
Last updated
2021-03-15

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

Conditions

Premature Ovarian Insufficiency

Interventions

POI-group:MHT

Sponsors

Beijing Obstetrics and Gynecology Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
10 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. aged less than 40 years old; 2. oligomenorrhea or menstruation stopped for at least 4 months; 3. serum FSH was more than 25 U/L at least twice(interval > 4 weeks).

Exclusion criteria

Exclusion criteria: 1. Pregnancy, abortion or lactation in the past month; 2. Thyroid and adrenal diseases; 3. Patients with polycystic ovary syndrome and hyperprolactinemia.

Design outcomes

Primary

MeasureTime frame
FSH;E2;LH;P;T;FT;PRL;AMH;SHGB;Transvaginal ultrasound;breast ultrasound;Bone Mineral Densitometer;—

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