Impact of an Early Warning System on the Prognosis of Patients With Hematological Malignancies Receiving Intensive Chemotherapy With or Without Hematopoietic Cell Transplantation.
NCT ID: NCT06409767
Last Updated: 2025-09-24
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
NA
2224 participants
INTERVENTIONAL
2025-04-10
2028-07-11
Brief Summary
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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 clarify the role of such a strategy.
In this study, the investigators will prospectively evaluate the implementation of the National Early Warning Score (NEWS), with systematic referral to the ICU in high-score patients, to improve the survival of patients receiving intensive chemotherapy in ten academic centers. This score is one of the most performant and most frequently used to predict organ failure. Its calculation only requires vital signs such as respiratory rate, peripheral oxygen saturation, need for oxygen therapy, body temperature, arterial pressure, heart rate, and level of consciousness. The investigators will therefore study the impact of ICU admission in patients with high NEWS in a randomized, controlled trial. A cluster randomization is planned in which the centers will be randomized between usual care (control group) and interventional care with transfer to the ICU in the event of a NEWS score ≥7 (interventional group). Each parameter used to calculate the NEWS will be collected at least three times a day by the attending nurse.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Interventional arm
Real-time calculation of the NEWS with ICU admission if NEWS ≥ 7.
The calculation of NEWS requires vital signs such as respiratory rate, peripheral oxygen saturation, need for oxygen therapy, body temperature, arterial pressure, heart rate, and level of consciousness. Each parameter used to calculate the NEWS will be collected least three times a day by the attending nurse.
Control arm
No interventions assigned to this group
Interventions
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Real-time calculation of the NEWS with ICU admission if NEWS ≥ 7.
The calculation of NEWS requires vital signs such as respiratory rate, peripheral oxygen saturation, need for oxygen therapy, body temperature, arterial pressure, heart rate, and level of consciousness. Each parameter used to calculate the NEWS will be collected least three times a day by the attending nurse.
Eligibility Criteria
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Inclusion Criteria
* Hospitalization in a protected unit of a hematology department for induction therapy of acute myeloid leukemia or acute lymphoblastic leukemia induction, intensive chemotherapy with autologous hematopoietic cell transplantation, allogeneic hematopoietic cell transplantation
* Expected length of stay in the hematology department of at least 7 days
* Patient with social security
* Signed informed consent form
Exclusion Criteria
* Pregnant, parturient or breastfeeding woman
* Person deprived of liberty by judicial or administrative decision
* Person under forced psychiatric care
* Person under legal protection
* Person unable to express consent
* Hospitalization for Chimeric Antigenic Receptor (CAR) T-cell therapy
18 Years
ALL
No
Sponsors
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University Hospital, Angers
OTHER_GOV
Responsible Party
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Locations
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Centre Hospitalier Amiens-Picardie
Amiens, , France
Centre Hospitalier Universitaire d'Angers
Angers, , France
Centre Hospitalier Universitaire Besancon
Besançon, , France
Centre Hospitalier Universitaire Brest
Brest, , France
Centre Hospitalier universitaire Nancy
Nancy, , France
Centre Hospitalier Universitaire Nantes
Nantes, , France
Centre Hospitalier Universitaire poitiers
Poitiers, , France
centre Hospitalier Universitaire Saint etienne
Saint-Etienne, , France
centre Hospitalier Universitaire Strasbourg
Strasbourg, , France
centre Hospitalier Universitaire Tours
Tours, , France
Countries
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Central Contacts
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Facility Contacts
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Maria-Pilar Gallego-Hernanz, PhD
Role: primary
Other Identifiers
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ID-RCB
Identifier Type: OTHER
Identifier Source: secondary_id
49RC23_0425
Identifier Type: -
Identifier Source: org_study_id
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