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Study identifier: NCT06513351 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Pragmatic Randomized Controlled Trial to Predict Postpartum Hemorrhage

Condition: Post Partum Hemorrhage  ·  Sponsor: Holly Ende

PhaseNA
Planned participants12500
Who can joinFemale, N/A to no upper limit
Healthy volunteersNo

About this study

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 with a provider-facing Best Practice Advisory (BPA) regarding currently recommended strategies triggered by an increased predicted risk, can improve perinatal outcomes. This study will compare the current category based risk assessment tool with a new, enhanced prediction model which calculates risk based on 21 factors, automatically updates as new information becomes available during labor and, if elevated, provides a provider-facing Best Practice Advisory (BPA) recommending consideration of strategies that are institutionally agreed to represent high-quality practice. Investigators hypothesize that the enhanced care approach will result in improved perinatal outcomes. The goal of the study is to improve the wellbeing of mothers during childbirth by harnessing the power of modern technology and data analysis.

This description comes directly from the study's public registry record.

Talk to the study team

Holly Ende, MD  ·  615-322-8476  ·  holly.ende@vumc.org

Tracie Baker, CCRP  ·  615-875-1852  ·  tracie.d.baker@vumc.org

Always discuss trial participation with your own doctor first.

Locations (1)

Vanderbilt University Medical CenterNashville, Tennessee, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06513351