Clinical trial Recruiting at 1 site Observational Ages 18 to 40 Women only

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.

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Quick facts

Study typeObservational
Ages18 Years to 40 Years
SexWomen only
Enrollment10000 (estimated)
SponsorThe First Affiliated Hospital of Zhengzhou University
Academic / other
Locations1 site (Zhengzhou, Henan)
StatusRecruiting
StartedJanuary 1, 2010
Main results expectedDecember 31, 2050
Study endsDecember 31, 2050
Registry record updatedJune 19, 2019
Trial IDNCT03991507 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.