A Pragmatic Randomized Controlled Trial to Predict Postpartum Hemorrhage
Not Applicable
Not yet recruiting
- Conditions
- Post Partum Hemorrhage
- Registration Number
- NCT06513351
- Lead Sponsor
- Holly Ende
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not yet recruiting
- Sex
- Female
- Target Recruitment
- 10000
Inclusion Criteria
Inclusion Criteria:<br><br> - All vaginal and cesarean deliveries occurring at Vanderbilt University Medical<br> Center<br><br>Exclusion Criteria:<br><br> - All patients will be randomized at the time of admission to the obstetric service.<br> Patients who are discharged prior to delivery will be excluded from subsequent<br> analysis. Any patients with a pre-delivery planned hysterectomy (for placenta<br> increta or percreta) will be excluded from the treatment algorithm and primary<br> analysis.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Numerical hierarchical composite score of postpartum morbidity and mortality at hospital discharge;Numerical hierarchical composite score of postpartum morbidity and mortality at 30 days postpartum
- Secondary Outcome Measures
Name Time Method