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NCT04141956: OHE-REA
Incidence of Use of High-Flow Nasal Cannula Oxygen Therapy in Intensive Care Units Patients
trial testing High-Flow Nasal Cannula in Oxygen Deficiency in 257 participants. Completed in 30 October 2020.
30 October 2020
Quick facts
| Lead sponsor | Nantes University Hospital |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 257 |
| Start date | 2 November 2019 |
| Primary completion | 30 October 2020 |
| Estimated completion | 30 October 2020 |
| Sites | 10 locations across France |
Drugs / interventions tested
- High-Flow Nasal Cannula
Conditions studied
- Oxygen Deficiency — all drugs for Oxygen Deficiency →
Sponsor
Nantes University Hospital
Who can join
Adults 18 to 99, any sex, with Oxygen Deficiency. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Patients with one or more organ failure (heart, lung) require hospitalization in intensive care where these failures can be managed. Nearly 30% of patients in intensive care units are hospitalized for acute respiratory distress (lung failure). This failure occurs in about 20% of postoperative patient, but it can also occur in the context of a pathology specific to the lung or after weaning of mechanical ventilation. It is therefore interesting to develop several techniques to provide oxygen to these patients with the aim in particular to avoid the use of intubation (insertion of a tube into the trachea to achieve artificial ventilation). For the past ten years, High-Flow Nasal Canula (HFNC) has developed. This technique reduces the need for intubation but the studies are contradictory, however they agree on its ease of use and the few risks associated with it. The principle of this technique is to deliver a humidified and heated gas mixture at a high rate through large nasal cannula. The advantage of this device is its non-invasive and the possibility of administering a large amount of oxygen. There is a certain craze for this oxygenation technique despite few scientific studies in the literature. However, it requires the expertise of the medical and paramedical team so as not to delay intubation. The investigators propose to carry out an observational study (without any modification of the usual practices) with epidemiological aim in order to make an inventory of the modes of use of the HFNC, in particular on its frequency of use and on its duration of use per patient hospitalized in intensive care. The investigators will recruit all HFNC patients in intensive care units (20 centers) (30 patients / center): 15 after weaning of mechanical ventilation and 15 others for other reasons. Patients will be followed every day and up to 48 hours after removal of the HFNC.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
High-flow nasal-cannula oxygen therapy in intensive-care-unit patients: a prospective multicenter observational cohort study (OHE-REA).
Compagne P, Ehrmann S, Jonas M, Morin J, et al · · 2026 · PMID 41735369 · DOI 10.1038/s41598-026-39969-4
Verify or expand the search:
- PubMed search for NCT04141956
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
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Related trials
Other trials of High-Flow Nasal Cannula
Trials testing the same drug.
- NCT07234188 — POM vs HFNC for Hypoxemia Prevention in Children · NA · recruiting
- NCT07384494 — High-flow Nasal Cannula Versus Conventional Oxygen During Awake Tracheal Intubation With Difficult Airways · NA · recruiting
- NCT07093372 — LMA vs High-flow Nasal Oxygen During ECT in Obese Patients · NA · not yet recruiting
- NCT06817603 — Procedural Oxygen Mask vs. High-flow Nasal Cannula for Hypoxemia Prevention During ERCP · NA · completed
- NCT06683677 — High Flow Nasal Cannula for Stabilization of Extremely Premature Infants · NA · not yet recruiting
Other recruiting trials for Oxygen Deficiency
Currently open trials in the same condition.
- NCT06475261 — Tissue Oximetry's Measurement in Cytoreductive Surgery With Hyperthermic Intraperitoneal Chemotherapy · recruiting
- NCT06404151 — Comparison of Oxygen Reserve Index and Regional Cerebral Oxygen Saturation Indetermining Hypoxia in Obese Patients · recruiting
Other Nantes University Hospital trials
Trials by the same sponsor.
- NCT07278661 — Preoperative Use of Romiplostim in Thrombocytopenic Patients Undergoing Cardiac Surgery. · Phase 2 · recruiting
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- NCT07467382 — GOAT (Gait Observation of Achilles Tendon) · not yet recruiting
- NCT07490379 — Comparison of the Efficacy of Transcranial Direct Current Stimulation at Home Versus in Hospital Settings in Patients Wi · NA · not yet recruiting
- NCT07423481 — Weight Trajectories and Predictive Factors After Semaglutide in Patients With Grade 3 and Complicated Obesity · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04141956 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Nantes University Hospital
- Last refreshed: 17 March 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04141956.
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