The clinical study of patients with poor ovarian response and premature ovarian insufficiency

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-17010945

Enrollment

Unknown

Registered

2017-03-21

Start date

2016-06-01

Completion date

Unknown

Last updated

2019-02-04

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

Conditions

poor ovarian response and premature ovarian insufficiency

Interventions

1:CoQ 10, estrogeon,progesteron

2:Without intervention

Eligibility

Sex/Gender

Female

Age

20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients with poor ovarian response or premature ovarian insufficiency

Exclusion criteria

Exclusion criteria: normal and high ovarian response, abnormal chromosome, pelvic operation, chemotherapy radiotherapy treament history

Design outcomes

Primary

Measure	Time frame
clinical pregnancy rate;abortion rate;Oocyte tetrieval rate;High quality embryo number;reproductive homoral level;	—

Countries

China

Contacts

Public ContactXumei Zhen

The Third Hospital of Peking Univestity

xmzhen1970@aliyun.com+86 13810766225

Outcome results

None listed

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