A Pragmatic Randomized Controlled Trial to Predict Postpartum Hemorrhage

Recruiting N/A Interventional Study
Post Partum Hemorrhage
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Sex
Female
Study type
Interventional
Purpose
Health Services Research
Participants needed
12,500 (estimated)
Sponsor
Holly Ende · Other
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About This Trial
This research project aims to enhance the safety of childbirth by using advanced computer models to predict the risk of postpartum hemorrhage (PPH). PPH is a significant concern for mothers during and after delivery. Current risk assessment tools are basic and do not adapt to changing conditions. This study will investigate whether a new and recently validated model for predicting PPH, combined w…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * All vaginal and cesarean deliveries occurring at Vanderbilt University Medical Center Exclusion Criteria: * All patients will be randomized at the time of admission to the obstetric service. Patients who are discharged prior to delivery will be excluded from subsequent analy…
Contacts

Holly Ende, MD

615-322-8476

holly.ende@vumc.org

CONTACT

Tracie Baker, CCRP

615-875-1852

tracie.d.baker@vumc.org

CONTACT