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

• Sponsor: Ain Shams University (Other)
• Overall Status: Completed
• CT.gov ID: NCT05617989
• Collaborator: (none)
• Enrollment: 30
• Location: 1
• Actual Duration (Months): 23.3
• Patients Per Site Per Month: 1.3

Study Details

Study Description

Brief Summary

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

Condition or Disease	Intervention/Treatment	Phase
Weaning Failure	Other: lung ultrasound

Study Design

• Study Type: Observational
• Actual Enrollment: 30 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: Role of Non-invasive Mechanical Ventilation and Diuretics in Improving Weaning Outcome of Patients With High Lung Ultrasound Score
• Actual Study Start Date: Apr 30, 2020
• Actual Primary Completion Date: Dec 4, 2021
• Actual Study Completion Date: Apr 10, 2022

Outcome Measures

Primary Outcome Measures

1. weaning failure ( number of patients) [48 hours]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 21 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Medicine Ain Shams University	Cairo		Egypt

Sponsors and Collaborators

• Ain Shams University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Mona Ammar, Assistant Professor, Ain Shams University
• ClinicalTrials.gov Identifier: NCT05617989
• Other Study ID Numbers: MD 243/2020
• First Posted: Nov 16, 2022
• Last Update Posted: Nov 16, 2022
• Last Verified: Nov 1, 2022

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Study Results

No Results Posted as of Nov 16, 2022