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NCT05289960 Clinical Trial

Lung Ultrasound Score and Weaning Outcome

Acute Respiratory Failure Clinical Trial

Official title:
Lung Ultrasound Score for Prediction of Weaning Outcome

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05289960
Other study ID # MS-490-2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2020
Est. completion date March 1, 2022

Study information
Verified date March 2022
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objectives: Failure of extubation of patients on mechanical ventilation is one of the common problems in the ICU. Aim of work: To evaluate the validity of lung ultrasound score in prediction of weaning outcomes and post-extubation distress.

Description:

Methods: A prospective observational study of 50 patients planned for extubation who passed a spontaneous breathing trial, lung ultrasound score and serum level of NT-PRO BNP were done to all patients at end of spontaneous breathing trial, and all patients were followed after extubation and monitored for oxygenation, re-intubation rate, ICU stay, and ICU mortality.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date March 1, 2022
Est. primary completion date February 28, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - 1. Patients age > 18 years 2. Patients intubated and mechanically ventilated for more than 48 hours in the intensive care unit and planned for extubation. Exclusion Criteria: - 1. Patients < or =18 years 2. Patients with left ventricular failure 3. Right ventricular failure 4. Pulmonary hypertension 5. Aortic valve disease 6. Hyperthyroidism 7. Tracheostomy

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• lung ultrasound
Lung ultrasound score was done at the end of SBT using curved array ultrasound probe 2-5 MHz, Siemens X300, Korea

Locations
Country Name City State
Egypt Cairo University Hospitals Cairo

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Extubation success number of participants that do not need for respiratory support neither NIV nor intubation for one week during ICU stay 48 hours
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