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

The recruitment status of this study is unknown because the information has not been verified recently.
Verified May 2013 by Mansoura University.
Recruitment status was  Recruiting
Sponsor:
Information provided by (Responsible Party):
Amr Mohamed Yassen, Mansoura University
ClinicalTrials.gov Identifier:
NCT01865019
First received: April 23, 2013
Last updated: May 26, 2013
Last verified: May 2013
History of Changes
  Purpose
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 Intervention
Living Donor Liver Transplantation Recipients
 Device: mechanical ventilation

Study Type: Observational [Patient Registry]
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Target Follow-Up Duration: 7 Days

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by Mansoura University:

Primary Outcome Measures:
  • oxygen tension [ Time Frame: during intraoperative period ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • decreased postoperative pulmonary complications [ Time Frame: one week postoperative ] [ Designated as safety issue: Yes ]

Other Outcome Measures:
  • improved intraoperative hemodynamics [ Time Frame: intraoperative ] [ Designated as safety issue: Yes ]
Estimated Enrollment: 60
Study Start Date: April 2013
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: October 2014 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
volume controlled
volume ontrolled ventilation
 Device: mechanical ventilation
pressure controlled
pressure controlled ventilation
 Device: mechanical ventilation

  Eligibility
Ages Eligible for Study:   Child, Adult, Senior
Genders Eligible for Study:   Both
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

Responsible Party: Amr Mohamed Yassen, PROFESSOR, Mansoura University
ClinicalTrials.gov Identifier: NCT01865019     History of Changes
Other Study ID Numbers: 1981  2013 
Study First Received: April 23, 2013
Last Updated: May 26, 2013
Health Authority: Egypt: faculty of medecine

ClinicalTrials.gov processed this record on September 29, 2016