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Pivotal, Prospective, Multi-centre, Single-arm Study to Evaluate the Safety and Effectiveness of Oli for Identification of Patients, During the Intrapartum Period, Who Are at Higher Risk of Developing Abnormal Postpartum Uterine Bleeding, Including Postpartum Haemorrhage

NCT06655207

Conditions
Female Urogenital Diseases and Pregnancy Complications, Hemorrhage, High Risk Pregnancy, +10 more
Locations
  • UC Health University of Colorado Hospital Denver, Colorado, United States
  • Woman's Hospital Baton Rouge, Louisiana, United States
  • Columbia University Irving Medical Center New York, United States
  • The Ohio State University Columbus, Ohio, United States
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