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Treatment Strategy in Patients With High-risk of Postextubation Distress in ICU Based on a Lung Ultrasound Score Versus Standard Strategy

NCT02123940 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 483

Last updated 2026-04-21

No results posted yet for this study

Summary

Prospective, randomized clinical multicentric study in ICU during weaning from mechanical ventilation.

Conditions

  • Adult Patients Ventilated More Than 48 h

Interventions

DEVICE

lung ultrasound score

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

Sponsors & Collaborators

  • Pitié-Salpêtrière Hospital

    collaborator OTHER

  • University Hospital, Grenoble

    collaborator OTHER

  • Hospices Civils de Lyon

    collaborator OTHER

  • Centre Hospitalier Universitaire de Saint Etienne

    collaborator OTHER

  • University Hospital, Marseille

    collaborator OTHER

  • University Hospital, Clermont-Ferrand

    lead OTHER

Principal Investigators

  • Sébastien PERBET · University Hospital, Clermont-Ferrand

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-02-28
Primary Completion
2018-08-25
Completion
2018-08-25

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02123940 on ClinicalTrials.gov