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

Clinical trial NCT06655207 · ACTIVE_NOT_RECRUITING

Trial details

NCT number: NCT06655207
Sponsor: Baymatob Operations Pty Ltd
Status: ACTIVE_NOT_RECRUITING
Phase: Not Applicable
Study type: INTERVENTIONAL

Post Partum Haemorrhage Maternal Care Patterns High Risk Pregnancy

Start date: 2025-08-06
Primary completion: 2026-06-26
Enrollment: 1000

View on ClinicalTrials.gov

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