Effect of Mannitol on Postreperfusion Syndrome During Living Donor Liver Transplant

NCT ID: NCT05277623

Last Updated: 2023-01-18

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

EARLY_PHASE1

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-04-04

Study Completion Date

2022-12-10

Brief Summary

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Postreperfusion syndrome during living liver transplants remains a serious concern for transplant anesthesiologists. This syndrome is responsible for decreases in systemic blood pressure, systemic vascular resistance, and cardiac output and can even lead to cardiac arrest. Delayed graft function and primary graft nonfunction are closely related to postreperfusion syndrome (Therefore, attenuating the syndrome during anesthesia is of great importance.

Detailed Description

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Conditions

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Liver Transplant Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Caregivers

Study Groups

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mannitol group

Group Type ACTIVE_COMPARATOR

Mannitol

Intervention Type DRUG

During the anhepatic phase, the patients in the mannitol group (30) will receive 1 g/kg

control group

Group Type PLACEBO_COMPARATOR

0.9% normal saline

Intervention Type OTHER

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

Intervention Type DRUG

0.9% normal saline

the same amount of 0.9% normal saline

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patients with end-stage liver disease who will undergo living donor transplantation.

Exclusion Criteria

* Patients with a history of portopulmonary hypertension.
* Hepatopulmonary syndrome.
* Cirrhotic cardiomyopathy.
* Hepatorenal syndrome types 1 and 2.
Minimum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

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Mona Ammar

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Medicine Ain Shams University

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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R 42/ 2022

Identifier Type: -

Identifier Source: org_study_id

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