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NCT05617989 Clinical Trial

Role of Non-invasive Mechanical Ventilation and Diuretics in Improving Weaning Outcome of Patients With High Lung Ultrasound Score

Weaning Failure Clinical Trial

Official title:
Role of Non-invasive Mechanical Ventilation and Diuretics in Improving Weaning Outcome of Patients With High Lung Ultrasound Score

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05617989
Other study ID # MD 243/2020
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 30, 2020
Est. completion date April 10, 2022

Study information
Verified date November 2022
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

patients who succeeded in SBT with high lung scores by ultrasound, non-invasive ventilation, and diuretic may have a role.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date April 10, 2022
Est. primary completion date December 4, 2021
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - age = 21 years of age - mechanical ventilation for more than 48 hrs - patients successfully passed according to the traditional weaning criteria - lung ultrasound score = 17. Exclusion Criteria: - Significant obstructive lung diseases - Obstructive sleep apnea - Interstitial lung disease - Neuromuscular disorders

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• lung ultrasound
non-invasive ventilation and diuretic

Locations
Country Name City State
Egypt Medicine Ain Shams University Cairo

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary weaning failure ( number of patients) 48 hours
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