Investigating health consequences in women with primary ovarian insufficiency
Official title: Prospective Cohort Study for Primary Ovarian Insufficient Patients in Clinical Reproductive Medicine Management System/Electronic Medical Record Cohort Database (CCRM/EMRCD)
Run by The First Affiliated Hospital of Zhengzhou University · NCT03989154 · Data updated 2026-11-12
This study is trying to learn more about the health effects of premature ovarian insufficiency in women by collecting health information and samples to see how it impacts their lives.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 40 Years |
| Sex | Women only |
| Enrollment | 10000 (estimated) |
| Sponsor | The First Affiliated Hospital of Zhengzhou University Academic / other |
| Locations | 1 site (Zhengzhou, Henan) |
| Status | Recruiting |
| Started | January 1, 2010 |
| Main results expected | December 31, 2050 |
| Study ends | December 31, 2050 |
| Registry record updated | June 19, 2019 |
| Trial ID | NCT03989154 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are women under 40 years of age who have experienced amenorrhea for at least four months and have specific hormonal test results indicating POI.
✕Probably not a fit
Patients who do not meet the age or hormonal criteria for primary ovarian insufficiency will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study focuses on women diagnosed with premature ovarian insufficiency (POI), a condition affecting fertility and characterized by specific hormonal imbalances. Conducted at the Reproductive Medical Center of the First Affiliated Hospital of Zhengzhou University, the study aims to collect biological samples, questionnaires, and health data to understand both short- and long-term health outcomes associated with POI. By utilizing a comprehensive database of reproductive health, the study seeks to provide valuable insights into the prognosis of women suffering from this condition.
Why it matters
Potential benefit: If successful, this study could enhance understanding of the health implications of primary ovarian insufficiency, leading to better management and treatment options for affected women.
How similar studies have gone: While studies on reproductive health conditions exist, this specific focus on the long-term health consequences of primary ovarian insufficiency is relatively novel and underexplored.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * younger than 40 years of age * at least four or more months of amenorrhea, two or more instances in which the serum FSH level is \> 40 U/L (i.e., two inspections at intervals of 1 month or more), with an oestradiol level of \<20pg/ml Exclusion Criteria: \-
Where it's running
-
Reproductive Medical Center, First Affiliated Hospital of Zhengzhou University
Zhengzhou, Henan, China Recruiting
Study contacts
- Study coordinator: Lanlan Fang, M.D.
- Email: fanglly@163.com
- Phone: 13673355291
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.