CompletedPhase 3

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

France483 participantsStarted 2014-02

Plain-language summary

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

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Adult patients ventilated more than 48 h * Stable respiratory and hemodynamic conditions for SBT * Consent of patients * Arterial line Exclusion Criteria: * severe COBP * Laryngeal dyspnea * Tracheostomy * Arrhythmia * No echogenicity * Paraplegia \>T8

What they're measuring

Incidence of postextubation distress

Timeframe: during 48 hour (at day 1)

Trial details

NCT IDNCT02123940

SponsorUniversity Hospital, Clermont-Ferrand

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2018-08-25

View on ClinicalTrials.gov More Adult Patients Ventilated More Than 48 h trials