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

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

Active, not recruiting · NCT06655207 · Registry updated 2026-07-01

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
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	Female Urogenital Diseases and Pregnancy Complications, Hemorrhage, Obstetric Labor Complications, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Postpartum Hemorrhage, Urogenital Diseases, Uterine Hemorrhage, pregnancy disorder, puerperal disorder	Active, not recruiting	Not applicable	2026-07-01		NCT06655207

3 results · Page 1 of 1

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Organizations	Linked trials
Baymatob Operations Pty Ltd	1
Royal Hospital For Women	3
Royal North Shore Hospital	24

7 results · Page 1 of 1

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Research sites	City	Country	Linked trials
Columbia University Irving Medical Center	New York	United States	234
Royal Hospital for Women	Randwick	Australia	2
Royal North Shore Hospital	St Leonards	Australia	50
The Ohio State University	Columbus	United States	191
UC Health University of Colorado Hospital	Denver	United States	1
UPMC Magee Womens Hospital	Pittsburgh	United States	5
Woman's Hospital	Baton Rouge	United States	28