Intrahospital Transport in Patients With High-flow Nasal Oxygenation: Prospective Observational Study
HospiFlow
1 other identifier
observational
175
1 country
4
Brief Summary
High-flow nasal oxygen therapy is commonly used in intensive care unit (ICU). Intra-hospital transfer of critical patients is frequent: 1) to perform diagnostic 2) between emergency room or medical wards and ICU. During theses transfers, oxygenation should be continued. There is high-flow nasal oxygen therapy for transport using an external battery. This mode of operation in transport mode allows about 30-45 min of autonomy. Intra-hospital transport under high-flow nasal oxygen therapy has been previously described on children. The objective of this study is to evaluate the occurrence of complications during intra-hospital transports under high-flow nasal oxygen of critical patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started May 2022
4 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 23, 2022
CompletedFirst Posted
Study publicly available on registry
April 5, 2022
CompletedStudy Start
First participant enrolled
May 28, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 4, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
May 4, 2024
CompletedDecember 23, 2025
December 1, 2025
1.9 years
March 23, 2022
December 22, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Incidence of severe adverse events during intra-hospital transport
To evaluate the incidence of severe adverse events during intra-hospital transport of patients treated with high-flow nasal oxygen surpervised by an ICU staff. Severe adverse event is defined by the occurrence of intubation during transport or severe hypoxemia defined as pulse oxygen saturation (SpO2 \< 80%) or cardiorespiratory arrest.
Up to 28 days
Secondary Outcomes (1)
Incidence of minor adverse events during intra-hospital transport
Up to 28 days
Interventions
Evaluation of the incidence and nature of adverse events during intra-hospital transport of patients undergoing high-flow nasal oxygen therapy provided by intensive care units
Eligibility Criteria
All patients requiring intra-hospital transfer on high-flow nasal oxygen therapy will be eligible to participate in the study
You may qualify if:
- Patient treated with high-flow nasal oxygen therapy before the intra-hospital transport prior to transport
- Requiring an intra-hospital transport (e.g., CT scan, OR, etc.) or inter-departmental transport supervised by the ICU team
- Nb: Once the patient is included in the study, any intra-hospital transport under high-flow nasal oxygen therapy will be analyzed until discharge from the intensive care unit and at until D28.
You may not qualify if:
- Under 18 years old
- Patient being under guardianship, tutorship or curatorship
- Pregnancy or breastfeeding
- Lack of social security number
- Refusal to participate in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (4)
Hospital Center of DAX
Dax, France
CH de Martigues
Martigues, France
CHU Orléans
Orléans, 45067, France
CH Bretagne Atlantique vannes-Auray
Vannes, 56017, France
Related Publications (1)
Nay MA, Bisson A, Auvet A, Delbove A, Berrouba A, Kamel T, Desgrouas M, Boulain T. Intra-hospital transport of adult critically ill patients treated with high flow nasal cannula oxygen: a prospective observational multicenter study. Ann Intensive Care. 2025 Jul 8;15(1):93. doi: 10.1186/s13613-025-01502-7.
PMID: 40629187DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mai-Anh NAY, Dr
CHU d'Orléans
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 23, 2022
First Posted
April 5, 2022
Study Start
May 28, 2022
Primary Completion
May 4, 2024
Study Completion
May 4, 2024
Last Updated
December 23, 2025
Record last verified: 2025-12