Evaluation of the Impact of Implementing a Patient Blood Management Protocol on the Transfusion Rate in Delivery Hemorrhage
NCT ID: NCT06916832
Last Updated: 2026-01-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
240 participants
OBSERVATIONAL
2024-12-23
2026-01-31
Brief Summary
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Since 2010, the WHO has defined the rational use of blood products as the 4th global priority, and the need for countries to reduce blood transfusion. It introduces the concept of Patient Blood Management (PBM). This is a set of measures designed to manage anemia and bleeding in surgical patients, while avoiding the need for transfusion. These measures include preoperative screening for anemia and martial deficiency, iron and vitamin supplementation, intraoperative bleeding control and optimization of postoperative blood balance. Recommended by several national programs, PBM has developed rapidly in orthopedic and cardiac surgery, where numerous studies have demonstrated its effectiveness, particularly in terms of transfusion savings. In obstetrics, however, the implementation of PBM remains less widespread, notably due to the difficulty of getting teams on board, and the absence of protocolization.
However, given the high prevalence of anemia in pregnant women, and the inherent risk of hemorrhage in all deliveries with potential recourse to blood transfusion, personalized optimization of PBM is a major challenge in obstetrics.
The PBM is currently being implemented in routine practice in the CHITS maternity department, in line with recommendations.
In this context, our research aims to assess the impact of this new approach. Our main hypothesis is that implementation of a PBM protocol would reduce the rate of transfusion in delivery hemorrhage.
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Detailed Description
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Conditions
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Study Design
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COHORT
OTHER
Study Groups
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Before protocol implementation
pregnant women who did not use the patient blood management protocol during their pregnancy. In other words, women who gave birth in 2023 and 2024.
No interventions assigned to this group
After protocol implementation
pregnant women who benefited from the patient blood management protocol during their pregnancy. In other words, women who gave birth in 2025.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Under legal protection
* Hemoglobinopathies
* Patient's refusal to participate in research
18 Years
FEMALE
No
Sponsors
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Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
OTHER
Responsible Party
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Principal Investigators
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Géraldine SLEHOHER-LHERIAU, MD
Role: STUDY_DIRECTOR
Centre Intercommunal Toulon-La Seyne sur Mer
Locations
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Centre Hospitalier Intercommunal de Toulon-La Seyne sur mer
Toulon, VAR, France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2024-CHITS-018
Identifier Type: -
Identifier Source: org_study_id
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