- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03921112
Role of Lung Ultrasound in Weaning From Mechanical Ventilation in Postoperative Neurosurgical ICU Patients
May 18, 2020 updated by: Amin Mohammed Alansary Amin Ahmed Helwa, Ain Shams University
Role of Lung Ultrasound in Weaning From Mechanical Ventilation in Postoperative Neurosurgical ICU Patients :Prospective , Randomized Double-blinded Study
The aim of this study is to demonstrate the role of lung ultrasound in weaning from mechanical ventilation in neurosurgical ICU patients compared to the ordinary tools as chest X-ray , ABG, rapid shallow breathing index, ventilator parameters.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
130
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Cairo, Egypt, 11591
- Ain Shams University Hospitals
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 70 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Mechanically ventilated patients
- ASAI ,ASAII, ASAIII
Exclusion Criteria:
- Patients or gurdians refuse
- Patients with pneumthorax
- Patients with pleural effusion
- Patients with surgical emphysema
- Glasco coma score more than 8
- Patients on high inotropic support
- patients with diaphragmatic paralysis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: QUADRUPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
ACTIVE_COMPARATOR: lung ultrasound
|
bedside lung ultrasound will be done for patients
chest X-ray , ABG, RSBI, Ventilator parameters will be done for all patients
|
ACTIVE_COMPARATOR: x-ray, ABG, RSBI, Vetilator parameters
|
chest X-ray , ABG, RSBI, Ventilator parameters will be done for all patients
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
success of weaning
Time Frame: success of weaning for 48 hours
|
trans-thoracic lung ultrasound will be done to patients to start weaning
|
success of weaning for 48 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Amin m Alansary, ain shams University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
April 3, 2019
Primary Completion (ACTUAL)
August 1, 2019
Study Completion (ACTUAL)
October 1, 2019
Study Registration Dates
First Submitted
April 17, 2019
First Submitted That Met QC Criteria
April 17, 2019
First Posted (ACTUAL)
April 19, 2019
Study Record Updates
Last Update Posted (ACTUAL)
May 19, 2020
Last Update Submitted That Met QC Criteria
May 18, 2020
Last Verified
May 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- FMASU R26/2019
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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