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

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

240 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-23

Study Completion Date

2026-01-31

Brief Summary

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According to the WHO, anemia is one of the ten most serious health problems in the world. During pregnancy, it affects 42% of women worldwide and 25% in France. It is associated with an increased risk of perinatal morbidity and mortality, and recourse to blood transfusion. The blood transfusion is itself also a source of thromboembolic morbidity and mortality, infectious diseases and pulmonary pathologies. In addition, the risk of hemorrhage, particularly during delivery, is inherent to all pregnancies and difficult to predict.

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.

Detailed Description

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From 1 January 2023 to 31 December 2025, the investigators conducted a single-center, before-and-after study at the maternity unit of the Sainte Musse hospital in Toulon (level IIB maternity unit). This is a retrospective observational study with a retrospective section covering the period before the implementation of the PBM protocol between 1 January 2023 and 31 December 2024. Then a prospective part covering the period after the implementation of the PBM protocol, from 1 January 2025 to 31 December 2025.

Conditions

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Delivery Hemorrhage

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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

* Any patient who has had a delivery hemorrhage, whatever the mode of delivery

Exclusion Criteria

* Minor
* Under legal protection
* Hemoglobinopathies
* Patient's refusal to participate in research
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status RECRUITING

Countries

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France

Central Contacts

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Asmaa JOBIC

Role: CONTACT

04 83 77 20 61 ext. +33

Facility Contacts

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Géraldine SLEHOHER-LHERIAU, MD

Role: primary

0494145913 ext. +33

Other Identifiers

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2024-CHITS-018

Identifier Type: -

Identifier Source: org_study_id

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