Health Trials

PPROM Registry (Preterm Premature Rupture of Membranes)

ConditionsFetal Membranes, Premature RupturePreterm Premature Rupture of the MembranesOligohydramniosPremature Birth
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age14-55
SponsorAmerican Alliance for pProm Support

About this trial

Preterm Premature Rupture of Membranes (PPROM) before 37 weeks of pregnancy is responsible for 40% of preterm births in the United States. The PPROM Registry aims to identify possible causes of PPROM, evaluate trends in expectant management, measure maternal and fetal care, and to review short term and long term outcomes of affected pregnancies and births.

Eligibility criteria

Qualifiers

Women diagnosed with Preterm Premature Rupture of Membranes (PPROM) prior to 37 weeks of pregnancy

Disqualifiers

Those without a clinical diagnosis or confirmation of PPROM in pregnancy

Diagnosis of PROM beyond 37 weeks of pregnancy

Trial design

Treatments tested in this trial

  • There is no intervention associated with this study.

Treatment groups

3,000 Participants
are divided into 1 treatment group

Sponsors and collaborators

American Alliance for pProm Support

Lead sponsor

Source ClinicalTrials.gov