Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Role of Lung Ultrasound in Weaning From Mechanical Ventilation in Postoperative Neurosurgical ICU Patients

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03921112
Recruitment Status : Active, not recruiting
First Posted : April 19, 2019
Last Update Posted : April 19, 2019
Sponsor:
Information provided by (Responsible Party):
Amin Mohammed Alansary Amin Ahmed Helwa, Ain Shams University

Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Intensive Care (ICU) Device: lung ultrasound Other: routine tools Not Applicable

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 130 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Role of Lung Ultrasound in Weaning From Mechanical Ventilation in Postoperative Neurosurgical ICU Patients :Prospective , Randomized Double-blinded Study
Actual Study Start Date : April 3, 2019
Estimated Primary Completion Date : August 1, 2019
Estimated Study Completion Date : October 1, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Ultrasound

Arm Intervention/treatment
Active Comparator: lung ultrasound Device: lung ultrasound
bedside lung ultrasound will be done for patients

Other: routine tools
chest X-ray , ABG, RSBI, Ventilator parameters will be done for all patients

Active Comparator: x-ray, ABG, RSBI, Vetilator parameters Other: routine tools
chest X-ray , ABG, RSBI, Ventilator parameters will be done for all patients




Primary Outcome Measures :
  1. success of weaning [ Time Frame: success of weaning for 48 hours ]
    trans-thoracic lung ultrasound will be done to patients to start weaning



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   20 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03921112


Locations
Layout table for location information
Egypt
Ain Shams University hospitals
Cairo, Egypt, 11591
Sponsors and Collaborators
Ain Shams University
Investigators
Layout table for investigator information
Principal Investigator: Amin m Alansary Ain Shams University

Layout table for additonal information
Responsible Party: Amin Mohammed Alansary Amin Ahmed Helwa, Assistant professor, Ain Shams University
ClinicalTrials.gov Identifier: NCT03921112     History of Changes
Other Study ID Numbers: FMASU R26/2019
First Posted: April 19, 2019    Key Record Dates
Last Update Posted: April 19, 2019
Last Verified: April 2019

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No