Prevalence of an Early Success of Non-invasive Ventilation in the Emergency Departement.
NCT ID: NCT06213623
Last Updated: 2024-01-23
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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NOT_YET_RECRUITING
500 participants
OBSERVATIONAL
2024-01-15
2024-01-27
Brief Summary
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The aim is to measure the prevalence of the absence of non-invasive ventilation success in the emergency department. The secondary objective is to measure the association between an absence of non-invasive ventilation success and outcomes and to identify risk factor of an absence of non-invasive ventilation success in the emergency department.
It's a prospective observationnal multicenter study in department of Initiative Recherche Urgences Study Groups from January 2024, 15th to January 2024, 20th. The Initiative Recherche Urgences is a research network set up on the initiative of the Société Française de Médecine d'Urgence, with the aim of promoting and coordinating multicentre research projects in the field of emergency medicine, during short inclusion periods.
The primary outcome is the proportion of patients who do not have an early success of non-invasive ventilation. The investigators measure the absence of success instead of failure because failure is defined by intubation and most of patients managed with non-invasive ventilation in an emergency department will not be intubated because of their age. The absence of success is defined by at least one of the following criteria measured at 1-hour: death, cardiorespiratory arrest, tracheal intubation, respiratory rate over 30 breaths/min, neurological impairment defined by a Glasgow coma scale \< 14, signs of increased work of breathing, haemodynamic failure (defined by mean arterial pressure \< 65 mmHg despite volumetric expansion and/or catecholamines), early stop of non-invasive ventilation due to intolerance. The investigators choose to measure at one hour because non-invasive ventilation is provided from one to two hours in the emergency department.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patient admitted in an intrahospital or pre-hospital emergency department
* Patient managed with non invasive ventilation
* No objection to the use of data
Exclusion Criteria
* Patient with a care limitation, instruction not to be reanimated.
* Contraindication to initiation of nonninvasive ventilation at the start of management (non-COPD coma\< 10 non-COPD, hemodynamic failure, incoercible vomiting)
* Patient who have low autonomy as defined by a WHO score ≥ 3 (bedridden for more than 50% of the day, not confined to it)
18 Years
ALL
No
Sponsors
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Poitiers University Hospital
OTHER
Responsible Party
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Principal Investigators
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Jeremie LESTIENNE, MD PHD
Role: PRINCIPAL_INVESTIGATOR
CHU Poitiers
Locations
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Poitiers University Hospital
Poitiers, , France
Countries
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Central Contacts
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Facility Contacts
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References
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Marjanovic N, Lestienne J, Balen F, Coisy F, Gerlier C, Guenezan J, Mimoz O; SFMU-IRU network. Prevalence, risk factors and consequences of early clinical deterioration under non-invasive ventilation in emergency department patients: a prospective, multicentre, observational study of the French IRU Network. Crit Care. 2025 Jun 3;29(1):224. doi: 10.1186/s13054-025-05430-7.
Other Identifiers
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VENTIRU
Identifier Type: -
Identifier Source: org_study_id
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