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Filters: Condition: The Primary Outcome of This Study Will be the Rate of Endometritis Clear all
Terminated Phase 4 Interventional Accepts healthy volunteers Results available

Treatment Utility of Postpartum Antibiotics in Chorioamnionitis

NCT01585129
View directory record Official record
Conditions
The Primary Outcome of This Study Will be the Rate of Endometritis
Interventions
Postpartum Antibiotics, No postpartum antibiotics
Drug
Lead sponsor
Washington University School of Medicine
Other
Eligibility
14 Years to 50 Years · Female only
Enrollment
80 participants
Healthy volunteers
Accepts healthy volunteers
Timeline
2010 – 2014
U.S. locations
2
States / cities
St Louis, Missouri
Source: ClinicalTrials.gov public record
Updated Jun 18, 2018 · Synced Jul 21, 2026, 5:23 PM EDT