Registry for Preterm Premature Rupture of Membranes
Patient Registry for Women Diagnosed With Preterm Premature Rupture of Membranes or PPROM During Pregnancy
This study is collecting information about pregnancies affected by early water breaking to see what causes it and how to improve care for both moms and babies.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 3000 (estimated) |
| Ages | 14 Years to 55 Years |
| Sex | Female |
| Sponsor | American Alliance for pProm Support Academic / other |
| Locations | 1 site (Denver, Colorado) |
| Trial ID | NCT02997345 on ClinicalTrials.gov |
What this trial studies
The PPROM Registry aims to gather comprehensive data on pregnancies affected by Preterm Premature Rupture of Membranes (PPROM) before 37 weeks. It seeks to identify potential causes of PPROM, evaluate management trends, and assess both maternal and fetal care practices. By analyzing short-term and long-term outcomes of affected pregnancies, the registry aims to fill gaps in current knowledge and improve care protocols. This observational study will provide a large cohort of data, which is currently lacking in existing literature.
Who should consider this trial
Good fit: Ideal candidates for this registry are women diagnosed with Preterm Premature Rupture of Membranes before 37 weeks of pregnancy.
Not a fit: Patients who do not have a clinical diagnosis of PPROM or those diagnosed with PROM beyond 37 weeks may not benefit from this registry.
Why it matters
Potential benefit: If successful, this registry could lead to improved management strategies and outcomes for pregnancies affected by PPROM.
How similar studies have performed: This registry represents a novel approach, as few recent studies have focused on PPROM with large sample sizes and comprehensive follow-up.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women diagnosed with Preterm Premature Rupture of Membranes (PPROM) prior to 37 weeks of pregnancy Exclusion Criteria: * Those without a clinical diagnosis or confirmation of PPROM in pregnancy * Diagnosis of PROM beyond 37 weeks of pregnancy
Where this trial is running
Denver, Colorado
- Www.Aapprom.Org/the-Registry — Denver, Colorado, United States (Recruiting)
Study contacts
- Study coordinator: Erin Thatcher
- Phone: (740) 837-7766
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.