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Effect of Mannitol on Postreperfusion Syndrome During Living Donor Liver Transplant

Effect of Mannitol on Postreperfusion Syndrome During Living Donor Liver Transplant: a Randomized Clinical Trial

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05277623
Enrollment
60
Registered
2022-03-14
Start date
2022-04-04
Completion date
2022-12-10
Last updated
2023-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Transplant Disorder

Brief summary

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.

Interventions

DRUGMannitol

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

OTHER0.9% normal saline

the same amount of 0.9% normal saline

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
mean arterial blood pressureone hour after reperfusionpostreperfusion mean blood pressure

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026