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Study identifier: NCT06409767 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Impact of an Early Warning System on the Prognosis of Patients With Hematological Malignancies Receiving Intensive Chemotherapy With or Without Hematopoietic Cell Transplantation.

Condition: Leukemia · Lymphoma · Multiple Myeloma  ·  Sponsor: University Hospital, Angers

PhaseNA
Planned participants2224
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Patients with hematologic malignancies requiring intensive chemotherapy are at risk for life-threatening complications. Organ failure may appear rapidly and delay in initiating life-sustaining interventions may result in increased mortality. This encourages great alertness although not all patients require close monitoring. It is therefore critical to identify which patients are the most at risk for clinical deterioration to consider increased surveillance in these patients. The benefit of early intensive care unit (ICU) admission, as soon as the first signs of organ dysfunction appear, must also be clarified. Such an intervention could increase survival of patients by close monitoring and early initiation of organ-specific interventions but could also be responsible for anxiety and increased use of ICU resources. Many teams have analyzed the impact of early warning systems (EWS) including vital signs to detect organ dysfunction early on. It has been shown that these EWS could positively impact survival in many medical fields (pre-hospital, medicine or surgery departments). A few retrospective studies have explored the impact of EWS in hematology, with overall good prediction for ICU admission and mortality. Until now, it has however not been formally demonstrated that early ICU admission, as soon as the first signs of organ dysfunction appear, could benefit patients with hematologic malignancies. A randomized controlled trial studying the impact of early intervention would …

This description comes directly from the study's public registry record.

Talk to the study team

Corentin Orvain, MD PhD  ·  02 41 35 36 37  ·  Corentin.Orvain@chu-angers.fr

Aurélie Hautefort  ·  02 41 35 36 37  ·  DRCI-Promotion-Interne@chu-angers.fr

Always discuss trial participation with your own doctor first.

Locations (10)

Centre Hospitalier Amiens-PicardieAmiens, FranceRecruiting
Centre Hospitalier Universitaire d'AngersAngers, FranceRecruiting
Centre Hospitalier Universitaire BesanconBesançon, FranceRecruiting
Centre Hospitalier Universitaire BrestBrest, FranceRecruiting
Centre Hospitalier universitaire NancyNancy, FranceRecruiting
Centre Hospitalier Universitaire NantesNantes, FranceRecruiting
Centre Hospitalier Universitaire poitiersPoitiers, FranceRecruiting
centre Hospitalier Universitaire Saint etienneSaint-Etienne, FranceRecruiting
centre Hospitalier Universitaire StrasbourgStrasbourg, FranceNot Yet Recruiting
centre Hospitalier Universitaire ToursTours, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06409767