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

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ClinicalTrials.gov Identifier: NCT01865019
Recruitment Status : Unknown
Verified May 2013 by Amr Mohamed Yassen, Mansoura University.
Recruitment status was:  Recruiting
First Posted : May 30, 2013
Last Update Posted : May 30, 2013
Sponsor:
Information provided by (Responsible Party):
Amr Mohamed Yassen, Mansoura University

Study Description
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
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

Condition or disease Intervention/treatment
Living Donor Liver Transplantation Recipients Device: mechanical ventilation

Study Design
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Study Type : Observational [Patient Registry]
Estimated Enrollment : 60 participants
Observational Model: Case Control
Time Perspective: Prospective
Target Follow-Up Duration: 7 Days
Study Start Date : April 2013
Estimated Primary Completion Date : October 2014
Estimated Study Completion Date : December 2014

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U.S. FDA Resources

Groups and Cohorts
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

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


Outcome Measures
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Primary Outcome Measures :
  1. oxygen tension [ Time Frame: during intraoperative period ]

Secondary Outcome Measures :
  1. decreased postoperative pulmonary complications [ Time Frame: one week postoperative ]

Other Outcome Measures:
  1. improved intraoperative hemodynamics [ Time Frame: intraoperative ]

Eligibility Criteria
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
living donor liver transplantation recipients
Criteria

Inclusion Criteria:

  • all living donor liver transplantation recipients scheduled

Exclusion Criteria:

  • Moderate to severe restrictive pulmonary functions
Contacts and Locations
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

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): NCT01865019


Locations
Egypt
Gastroenterology center Recruiting
Mansoura, Dakahleya, Egypt
Contact: Amr M Yassen, Professor    01001497044 ext 002    amryassen@hotmail.com   
Principal Investigator: Al-refaey a KANDEEL, MASTER         
Sponsors and Collaborators
Mansoura University
More Information
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Responsible Party: Amr Mohamed Yassen, PROFESSOR, Mansoura University
ClinicalTrials.gov Identifier: NCT01865019     History of Changes
Other Study ID Numbers: 1981
2013 ( Other Identifier: GASTROENTEROLOGY CENTER LIVER TRANSPLANTATION ANESTHESIA TEAM )
First Posted: May 30, 2013    Key Record Dates
Last Update Posted: May 30, 2013
Last Verified: May 2013