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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04704596
Other study ID # FMASU R 127/2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 16, 2020
Est. completion date January 20, 2022

Study information

Verified date July 2022
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 evaluate The role of transthoracic lung US as a clinical tool in Comparison to dynamic lung compliance for detection of optimum PEEP for obese patients undergoing laparoscopic gastric sleeve surgery.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date January 20, 2022
Est. primary completion date January 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - physical status American Society of Anesthesiologist(ASA) I or II Exclusion Criteria: - Patients refuse ASA physical status more > II - Patients with pre-existing significant pulmonary disease with abnormalities in spirometry, previous lung surgery, home oxygen therapy and signi?cant cardiac dysfunction. - Patients with pulmonary hypertension.

Study Design


Related Conditions & MeSH terms

  • Mechanical Ventilation During Anesthesia

Intervention

Device:
anesthesia ventilator machine
dynamic lung compliance measurements will be used for detection of the optimum PEEP after alveolar recruitment
lung ultrasound
lung ultrasound views will be used for detection of the optimum PEEP after alveolar recruitment

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 detection of the optimum PEEP which is measured in mmHg the optimum PEEP will be detected after alveolar recruitment either by dynamic lung compliance or by lung ultarsound views intraoperative period
Secondary prevention of postoperative pulmonary complications patients will be monitored for detection of postoperative pulmonary complictaios as atelectasis , pneumothorax , respiratory failure 1st 24 hour