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NCT02022839 Clinical Trial

Role of Lung Ultrasound in Predicting Weaning Outcomes

Ultrasonography Clinical Trial

Official title:
B-lines at Lung Ultrasound Predicts Weaning Failure From Mechanical Ventilation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02022839
Other study ID # 2010/125
Secondary ID
Status Completed
Phase N/A
First received April 27, 2011
Last updated December 22, 2013
Start date December 2010
Est. completion date March 2013

Study information
Verified date December 2013
Source Hospital Moinhos de Vento
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Observational [Patient Registry]

Clinical Trial Summary

We aimed to verify the potencial role of bedside lung ultrasound findings of critically ill patients candidates to liberation from mechanical ventilation in predicting weaning outcomes. The analysis will be taken in two times: immediately before and at the and spontaneous breathing trial.

Recruitment information / eligibility
Status Completed
Enrollment 250
Est. completion date March 2013
Est. primary completion date March 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Invasive mechanical ventilation > 24 hours

- Eligibility to weaning from mechanical ventilation

Exclusion Criteria:

- Tracheostomy

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Brazil Hospital Moinhos de Vento Porto Alegre Rio Grande do Sul

Sponsors (1)
Lead Sponsor Collaborator
Hospital Moinhos de Vento

Country where clinical trial is conducted

Brazil, 

Outcome
Type Measure Description Time frame Safety issue
Primary Weaning Failure Participants will be followed up til weaning success or weaning failure at the end of spontaneous breathing trial. In case of weaning success, then they will be followed for more 48 hours to detect extubation failure. No
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