Investigating health outcomes in women with Polycystic Ovarian Syndrome
Prospective Cohort Study for PCOS Patients in Clinical Reproductive Medicine Management System/Electronic Medical Record Cohort Database (CCRM/EMRCD)
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 |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 18 Years to 40 Years |
| Sex | Female |
| Sponsor | The First Affiliated Hospital of Zhengzhou University Academic / other |
| Locations | 1 site (Zhengzhou, Henan) |
| Trial ID | NCT03991507 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are women diagnosed with PCOS according to The Rotterdam diagnostic criteria.
Not a fit: Patients without a diagnosis of PCOS or those who do not meet the inclusion criteria will not benefit from this study.
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 performed: While studies on PCOS are common, this specific approach utilizing a comprehensive database for long-term health outcomes is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * PCOS patients diagnosed with The Rotterdam diagnostic criteria. Exclusion Criteria: \-
Where this trial is running
Zhengzhou, Henan
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.