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| ID | Type | Description | Link |
|---|---|---|---|
| 2013-A01458-37 |
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| Name | Class |
|---|---|
| Pitié-Salpêtrière Hospital | OTHER |
| University Hospital, Grenoble | OTHER |
| Hospices Civils de Lyon | OTHER |
| Centre Hospitalier Universitaire de Saint Etienne |
Prospective, randomized clinical multicentric study in ICU during weaning from mechanical ventilation.
Prospective randomized clinical multicentric study on ICU comparing a treatment strategy (nasal humidified high flow therapy and Noninvasive Ventilation) in patients with high-risk of postextubation distress in ICU based on a Lung Ultrasound Score VERSUS standard strategy
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| nasal humidified high flow therapy | Experimental | Prospective randomized clinical multicentric study on ICU comparing a treatment strategy (nasal humidified high flow therapy and Noninvasive Ventilation) in patients with high-risk of postextubation distress in ICU based on a Lung Ultrasound Score VERSUS standard strategy |
|
| standard strategy | Other | Prospective randomized clinical multicentric study on ICU comparing a treatment strategy (nasal humidified high flow therapy and Noninvasive Ventilation) in patients with high-risk of postextubation distress in ICU based on a Lung Ultrasound Score VERSUS standard strategy |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| lung ultrasound score | Device | Prospective randomized clinical multicentric study on ICU comparing a treatment strategy (nasal humidified high flow therapy and Noninvasive Ventilation) in patients with high-risk of postextubation distress in ICU based on a Lung Ultrasound Score VERSUS standard strategy |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of postextubation distress | postextubation period requiring a ventilatory support (reintubation or curative Noninvasive ventilation). | during 48 hour (at day 1) |
| Measure | Description | Time Frame |
|---|---|---|
| Number of ventilator-free-days | at day 1 (after extubation) | |
| Length of stay in ICU | at day 1 | |
| Mortality in ICU |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Sébastien PERBET | University Hospital, Clermont-Ferrand | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU de Clermont-Ferrand | Clermont-Ferrand | 63003 | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 39593129 | Result | Rouby JJ, Perbet S, Quenot JP, Zhang M, Andreu P, Assefi M, Gao Y, Deransy R, Lyu J, Arbelot C, An Y, Monsel A, Jing X, Guerci P, Qian C, Malbouisson L, Morand D, Puybasset L, Futier E, Constantin JM, Pereira B; WIN IN WEAN Study Group. Weaning of non COPD patients at high-risk of extubation failure assessed by lung ultrasound: the WIN IN WEAN multicentre randomised controlled trial. Crit Care. 2024 Nov 26;28(1):391. doi: 10.1186/s13054-024-05166-w. |
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| OTHER |
| University Hospital, Marseille | OTHER |
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| at day 1 |
| Extubation failure | Extubation failure within the 7 days following planned extubation | at day 7 |