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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. The completion date has passed and the status has not been verified in more than two years.
Verified May 2013 by Amr Mohamed Yassen, Mansoura University.
Recruitment status was: Recruiting
Recruitment status was: Recruiting
Sponsor:
Mansoura University
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
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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:
Further study details as provided by Amr Mohamed Yassen, Mansoura University:
Primary Outcome Measures:
- oxygen tension [ Time Frame: during intraoperative period ]
Secondary Outcome Measures:
- decreased postoperative pulmonary complications [ Time Frame: one week postoperative ]
Other Outcome Measures:
- improved intraoperative hemodynamics [ Time Frame: intraoperative ]
| 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 |
| 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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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
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 ( Other Identifier: GASTROENTEROLOGY CENTER LIVER TRANSPLANTATION ANESTHESIA TEAM ) |
| Study First Received: | April 23, 2013 |
| Last Updated: | May 26, 2013 |
ClinicalTrials.gov processed this record on June 27, 2017