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Establishing the Diagnosis Standard and Analysis the Risk Factors of POI in Chinese Women

Primary Ovarian Insufficiency Clinical Trial

Official title:
Establishing the Diagnosis Standard and Analysis the Risk Factors of Premature Ovarian Insufficiency in Chinese Women： Multi-center, Prospective,Observational Study

Clinical Trial Summary

The study aims to establishing the diagnosis standard of POI and analyzing the risk factors in Chinese women.

Clinical Trial Description

Premature ovarian insufficiency (POI) is a clinical syndrome defined by loss of ovarian activity before the age of 40 years. The POI guideline development group of ESHRE recommends the following diagnostic criteria: oligo/amenorrhea for at least 4 months and an elevated follicle stimulating hormone (FSH) level ＞25 mIU/mL on two occasion ＞4 weeks apart. But there still no diagnosis standard of POI in Chinese.The study aims to establishing the diagnosis standard of POI and analyzing the risk factors in Chinese women. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03518918
Study type Observational
Source Nanfang Hospital of Southern Medical University
Contact Shi-ling Chen, M.D, Ph.D
Phone +86-020-62787604
Email chensl_92@163.com
Status Recruiting
Phase
Start date September 1, 2016
Completion date December 1, 2021
View Details
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