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Clinical Trials in Belgium / NCT06560164
Recruiting Not applicable

Restrictive Versus Liberal Thresholds for RBC Transfusion in ECMO

NCT06560164 · tracked via the Priya Life Science Belgium tracker
Phase
Not applicable
Started
2024-11-26
Last updated
2026-08-14

Condition(s) studied

TransfusionRed Blood CellExtracorporeal Membrane OxygenationAnemiaECMO

Investigational drug(s) / intervention(s)

Red Blood Cell transfusion

Red Blood Cell transfusion: When the appropriate Hb threshold is reached, patients in each group will have one unit of RBC administered at a time. Within 3 hours after the transfusion, a repeat Hb concentration will be measured. Each group will only be transfused when their Hb level falls below the transfusion threshold. In case of a outlier measurement, clinicians are advised to repeat the measurement. The RBC transfusion must take place within 4 hours when the Hb trigger was measured.

Study summary

Rationale: In patients supported with extracorporeal membrane oxygenation (ECMO), transfusion of red blood cells (RBC) is very common. This is possibly due to the application of liberal thresholds and the lack of evidence-based guidelines. Although RBC transfusion can be lifesaving, it is also a risk-bearing intervention with substantial risk for morbidity and mortality in this critically ill population. Also, with increasing scarcity, RBC transfusions are becoming more expensive. Furthermore, in the past decades it has been shown in several critically ill patient populations - not on ECMO - that maintaining a restrictive hemoglobin (Hb) threshold for RBC transfusion is non-inferior, including in cardiothoracic surgery, acute myocardial infarction and septic shock. Therefore, the investigators hypothesize that a restrictive transfusion threshold for RBC is safe to apply in patients on ECMO in comparison with a liberal transfusion threshold.

Objective: The primary objective of this trial is to study in a prospective randomized comparison whether a restrictive RBC transfusions strategy is non-inferior compared to a liberal strategy in patients on ECMO with respect to 90-day mortality.

Study design: Prospective multi-center randomized controlled non-inferiority trial.

Study population: Patients, 18 years or older, receiving ECMO.

Intervention: Restrictive RBC transfusion threshold: in case the Hb transfusion trigger of 7.0 g/dL (4.3 mmol/L) is reached, 1 RBC unit at a time will be transfused. The aimed Hb target range of the restrictive/intervention group will be 7.1 - 9.0 g/dL (4.3 - 5.6 mmol/L). Liberal RBC transfusion threshold: in case the Hb transfusion trigger of 9.0 g/dL (5.6 mmol/L) is reached, 1 RBC unit at a time will be transfused. Target range of the liberal group is defined as Hb 9.1 - 11.0 g/dL

Main study parameters/endpoints: The primary outcome parameter is 90-day all-cause mortality.

Secondary outcomes include: 1) proportion of patients on ECMO exposed to allogeneic RBC transfusion; 2) RBC volume infused per patient during ECMO; 3) reasons for RBC transfusion other than Hb triggers; 4) transfusion reactions; 5) time on ECMO; 6) length of hospital- and ICU-stay; 7) in-ICU morbidity; 8) quality of life (QoL), iMTA Medical Consumption Questionnaire (iMCQ) and Productivity Cost Questionnaire (iPCQ) at 3, 6, 9, and 12 months; 9) costs related to a) transfusion, b) hospital admission and c) transfusion-related sequelae.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient is aged 18 years or older; * Is receiving ECMO; * (Deferred) informed consent. Exclusion Criteria: * Not expected to survive for 24 hours when assessed; * Inability to receive blood products; * (Known) decline to blood transfusions (e.g., Jehovah's Witnesses); * Extracorporeal carbon dioxide removal (ECCO2R) using low blood flow devices or pumpless devices (i.e., MINILUNG ®, PrismaLung+); * Received ECMO over 48h before screening for eligibility.

Primary outcome measure(s)

Trial sites (14)

FacilityCityRegionStatus
MedUni Wien Vienna State of Vienna Recruiting
Hôpital Erasme Brussels Brussels Capital Recruiting
KU Leuven, medical IC Leuven Flemish Brabant Recruiting
KU Leuven, surgical IC Leuven Flemish Brabant Recruiting
CHU Charleroi Charleroi Hainaut Recruiting
Medisch Spectrum Twente (MST) Enschede Drenthe Recruiting
Radboudumc Nijmegen Gelderland Not Yet Recruiting
Maastricht Universitair Medisch Centrum+ (MUMC+) Maastricht Limburg Recruiting
Amsterdam UMC, location AMC Amsterdam North Holland Recruiting
Universitair Medisch Centrum Groningen (UMCG) Groningen Provincie Groningen Recruiting
Leids Universitair Medisch Centrum (LUMC) Leiden South Holland Recruiting
Erasmus MC Rotterdam South Holland Recruiting
St. Antonius Ziekenhuis Nieuwegein Utrecht Recruiting
Karolinska Universtiy Hospital Stockholm Stockholm County Recruiting

More Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) trials in Belgium

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06560164 on ClinicalTrials.gov ↗ ← All trials in Belgium