Skip to content

Establishment of an early diagnosis and intervention system for premature ovarian dysfunction

Establishment of an early diagnosis and intervention system for premature ovarian dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070044
Enrollment
Unknown
Registered
2023-03-31
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Premature ovarian insufficiency

Interventions

PRP Group:PRP intra-ovarian injection
Conventional treatment group:Conventional POI treatment

Sponsors

Women's Hospital School of Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: All the included subjects met the following inclusion criteria: ?=18 years old, < 40 years old; (2) The patient voluntarily accepted clinical observation and signed informed consent; ? Patients had no previous diagnosis of POI or had to stop POI-related therapy for more than 3 months.

Exclusion criteria

Exclusion criteria: History of bilateral ovariectomy; There are contraindications of fingertip blood collection, such as local skin infection and coagulopathy; There are contraindications of POI treatment; Or patients judged by the investigator to be unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
anti-Müllerian hormone;Follicle-stimulating Hormone;pregancy rate;live birth rate;

Secondary

MeasureTime frame
estrogen;Antral follicle count;abortion rate;egg retrival number;zygote number;success rate of embryo transfer;

Countries

China

Contacts

Public ContactWu Ruijin

Women's Hospital School of Zhejiang University

wurj@zju.edu.cn13757187083

Outcome results

None listed

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