Last updated: February 12, 2025
Sponsor: Holly Ende
Overall Status: Active - Recruiting
Phase
N/A
Condition
Hemorrhage
Treatment
Novel PPH Risk Prediction Model - Comparator Arm B
Clinical Study ID
NCT06513351
240187
Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- All vaginal and cesarean deliveries occurring at Vanderbilt University MedicalCenter
Exclusion
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 subsequentanalysis. Any patients with a pre-delivery planned hysterectomy (for placentaincreta or percreta) will be excluded from the treatment algorithm and primaryanalysis.
Study Design
Total Participants: 10000
Treatment Group(s): 1
Primary Treatment: Novel PPH Risk Prediction Model - Comparator Arm B
Phase:
Study Start date:
January 01, 2025
Estimated Completion Date:
July 31, 2027
Study Description
Connect with a study center
Vanderbilt University Medical Center
Nashville, Tennessee 37212
United StatesActive - Recruiting
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