Registry for Preterm Premature Rupture of Membranes

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• Www.Aapprom.Org/the-Registry
  Denver, Colorado, United States Recruiting

Study contacts

• Study coordinator: Erin Thatcher
• Phone: (740) 837-7766

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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.