Effect of Mannitol on Postreperfusion Syndrome During Living Donor Liver Transplant
NCT ID: NCT05277623
Last Updated: 2023-01-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
EARLY_PHASE1
60 participants
INTERVENTIONAL
2022-04-04
2022-12-10
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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mannitol group
Mannitol
During the anhepatic phase, the patients in the mannitol group (30) will receive 1 g/kg
control group
0.9% normal saline
the same amount of 0.9% normal saline
Interventions
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Mannitol
During the anhepatic phase, the patients in the mannitol group (30) will receive 1 g/kg
0.9% normal saline
the same amount of 0.9% normal saline
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Hepatopulmonary syndrome.
* Cirrhotic cardiomyopathy.
* Hepatorenal syndrome types 1 and 2.
16 Years
ALL
No
Sponsors
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Ain Shams University
OTHER
Responsible Party
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Mona Ammar
Assistant Professor
Locations
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Medicine Ain Shams University
Cairo, , Egypt
Countries
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Other Identifiers
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R 42/ 2022
Identifier Type: -
Identifier Source: org_study_id
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