Pressure Controlled Versus Volume Controlled Mechanical Ventilation During Anesthesia for Living Donor Liver Transplantation Recipients

May 26, 2013 updated by: Amr Mohamed Yassen, Mansoura University
pressure controlled ventilation will improve oxygenation indices , hemodynamics during anesthesia for living donor liver transplantation recipients ,improving postoperative graft function and decreasing postoperative pulmonary complications

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Anticipated)

60

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

  • Egypt
    • Dakahleya
      • Mansoura, Dakahleya, Egypt
        • Recruiting
        • Gastroenterology center
        • Contact:
        • Principal Investigator:
          • Al-refaey a KANDEEL, MASTER

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

living donor liver transplantation recipients

Description

Inclusion Criteria:

  • all living donor liver transplantation recipients scheduled

Exclusion Criteria:

  • Moderate to severe restrictive pulmonary functions

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
volume controlled
volume ontrolled ventilation
Device: mechanical ventilation
pressure controlled
pressure controlled ventilation
Device: mechanical ventilation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
oxygen tension
Time Frame: during intraoperative period
during intraoperative period

Secondary Outcome Measures

Outcome Measure
Time Frame
decreased postoperative pulmonary complications
Time Frame: one week postoperative
one week postoperative

Other Outcome Measures

Outcome Measure
Time Frame
improved intraoperative hemodynamics
Time Frame: intraoperative
intraoperative

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Mansoura 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

April 1, 2013

Primary Completion (Anticipated)

October 1, 2014

Study Completion (Anticipated)

December 1, 2014

Study Registration Dates

First Submitted

April 23, 2013

First Submitted That Met QC Criteria

May 26, 2013

First Posted (Estimate)

May 30, 2013

Study Record Updates

Last Update Posted (Estimate)

May 30, 2013

Last Update Submitted That Met QC Criteria

May 26, 2013

Last Verified

May 1, 2013

More Information

Terms related to this study

Other Study ID Numbers

  • 1981
  • 2013 (Other Grant/Funding Number: Food Innovation Center)

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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