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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03921112
Other study ID # FMASU R26/2019
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 3, 2019
Est. completion date October 1, 2019

Study information

Verified date May 2020
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 130
Est. completion date October 1, 2019
Est. primary completion date August 1, 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years to 70 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Egypt Ain Shams University hospitals 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 success of weaning trans-thoracic lung ultrasound will be done to patients to start weaning success of weaning for 48 hours
See also
  Status Clinical Trial Phase
Completed NCT05118529 - Physiological Response and Experience Between Sitting in Bed and Sitting in a Chair in ICU N/A