Investigating health outcomes in women with Polycystic Ovarian Syndrome
Official title: Prospective Cohort Study for PCOS Patients in Clinical Reproductive Medicine Management System/Electronic Medical Record Cohort Database (CCRM/EMRCD)
Run by The First Affiliated Hospital of Zhengzhou University · NCT03991507 · Data updated 2026-11-12
This study looks at the health effects of Polycystic Ovarian Syndrome in women to better understand how it impacts their lives now and in the future.
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 | NCT03991507 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are women diagnosed with PCOS according to The Rotterdam diagnostic criteria.
✕Probably not a fit
Patients without a diagnosis of PCOS or those who do not meet the inclusion criteria 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 Polycystic Ovarian Syndrome (PCOS) to explore both short- and long-term health consequences. Conducted at the Reproductive Medical Center of the First Affiliated Hospital of Zhengzhou University, the study utilizes a comprehensive database that includes biological samples, questionnaires, and health data. By recruiting PCOS participants, the study aims to gather evidence that could inform prognosis and management of the condition.
Why it matters
Potential benefit: If successful, this study could enhance understanding of PCOS and improve health outcomes for affected women.
How similar studies have gone: While studies on PCOS are common, this specific approach utilizing a comprehensive database for long-term health outcomes is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * PCOS patients diagnosed with The Rotterdam diagnostic criteria. 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.