Overview Postpartum Hemorrhage Prevention in Patients With Preeclampsia (PHP3 Study) Status: Completed Trial end date: 2019-07-17 Target enrollment: Participant gender: Summary Evaluation of the efficacy of postpartum 24 hour oxytocin infusion to reduce blood loss in patients with pre-eclampsia (PE) Phase: Early Phase 1 Details Lead Sponsor: University of Colorado, DenverTreatments: Oxytocin