MedTrace Logo

CoPPer Study - Complications of Polycystic Ovary Syndrome (PCOS) Pregnancy: Evaluating Risk

NCT00821379 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2012-12-20

No results posted yet for this study

Summary

The CoPPer study is a follow-up study of women diagnosed with Polycystic Ovary Syndrome (PCOS). Women will be included pre-conceptional and followed-up until after delivery. The investigators will design a multivariate prediction model of pregnancy outcome in women with PCOS with the intention to define intervention strategies for the future.

Conditions

  • Pregnancy Complications
  • Delivery Complications
  • Neonatal Complications

Sponsors & Collaborators

  • The Queen Elizabeth Hospital

    collaborator OTHER

  • Erasmus Medical Center

    collaborator OTHER

  • Amsterdam UMC, location VUmc

    collaborator OTHER

  • UMC Utrecht

    lead OTHER

Principal Investigators

  • Bart CJ Fauser, MD PhD · UMC Utrecht

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2011-01-31
Completion
2012-09-30

Countries

  • Netherlands

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00821379 on ClinicalTrials.gov