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.
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