Pressure Controlled Versus Volume Controlled Mechanical Ventilation During Anesthesia for Living Donor Liver Transplantation Recipients
2 other identifiers
observational
60
1 country
1
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Apr 2013
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2013
CompletedFirst Submitted
Initial submission to the registry
April 23, 2013
CompletedFirst Posted
Study publicly available on registry
May 30, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2014
CompletedMay 30, 2013
May 1, 2013
1.5 years
April 23, 2013
May 26, 2013
Conditions
Outcome Measures
Primary Outcomes (1)
oxygen tension
during intraoperative period
Secondary Outcomes (1)
decreased postoperative pulmonary complications
one week postoperative
Other Outcomes (1)
improved intraoperative hemodynamics
intraoperative
Study Arms (2)
volume controlled
volume ontrolled ventilation
pressure controlled
pressure controlled ventilation
Interventions
Eligibility Criteria
living donor liver transplantation recipients
You may qualify if:
- all living donor liver transplantation recipients scheduled
You may not qualify if:
- Moderate to severe restrictive pulmonary functions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Gastroenterology center
Al Mansurah, Dakahlia Governorate, Egypt
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Target Duration
- 7 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PROFESSOR
Study Record Dates
First Submitted
April 23, 2013
First Posted
May 30, 2013
Study Start
April 1, 2013
Primary Completion
October 1, 2014
Study Completion
December 1, 2014
Last Updated
May 30, 2013
Record last verified: 2013-05