Digital vs. Speculum Exams for PPROM
Recruiting
N/A
Interventional Study
PPROM
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Sex
- Female
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 86 (estimated)
- Sponsor
- Washington University School of Medicine · Other
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About This Trial
After preterm prelabor rupture of membranes (PPROM)\[breaking of the amniotic sac prior to 37 weeks gestation in pregnancy\], patients are recommended for inpatient admission and close monitoring for complications including preterm labor, intraamniotic infection (infection of the sac around the baby), and placental abruption (separation of the placenta from wall of the uterus). When evaluation of …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 22 weeks 0 days gestation to 33 weeks 5 days gestation
* Clinical or laboratory confirmation of PPROM
* At least 8 hours after rupture event
* English speaking
Notably, for patients \<25 weeks, approach for enrollment will be deferred until after the patient has discussed the…
Contacts