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Evaluation of the Effect of Lung Recruitment and Positive End- Expiratory Pressure (PEEP) on Anesthesia Induced Atelectasis Using Lung Ultrasound

NCT03069157 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2018-01-25

No results posted yet for this study

Summary

Atelectasis is a side effect of general anesthesia which can be found in all types of interventions and patients of all ages.1-3 The reported incidence of anesthesia- induced atelectasis in children varies, ranging from 12 to 42% in sedated and nonintubated patients 5, 6 and from 68 to 100% in children with general anesthesia with tracheal intubation or laryngeal mask.

The aim of this work is to evaluate the effect of lung recruitment on anesthesia induced atelectasis using intraoperative lung ultrasound.

Objectives

* To determine the effect of recruitment on anesthesia induced atelectasis using lung ultrasound.
* To Estimate the change of Pao2 with anesthesia induced lung atelectasis.
* To Estimate the change of Pao2 with lung recruitment.
* To evaluate the feasibility of use of lung ultrasound as a tool to guide optimum lung recruitment.

Conditions

  • Anesthesia Induced Atelectasis

Interventions

PROCEDURE

lung recruitment maneuver

lung recruitment manoeuvre will be performed in patients using continuous positive airway pressure( CPAP) (30) cm H2O for (40) seconds after induction of anesthesia then patient will be converted to pressure controlled mode again with PEEP 5 cm H2O

Sponsors & Collaborators

  • Cairo University

    collaborator OTHER

  • Kasr El Aini Hospital

    lead OTHER

Principal Investigators

  • Iman R Abdel- Aal, Professor · Anesthesia department , Cairo university

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
1 Year
Max Age
4 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-03-08
Primary Completion
2017-11-15
Completion
2017-11-15

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03069157 on ClinicalTrials.gov