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Impact of Dexmedetomidine on Acute Kidney Injury Following Living Donor Liver Transplantation

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StatusRecruiting
Sponsors
Asan Medical Center
Collaborators
Kyongbo Pharmaceutical

Keywords

Abstract

Acute kidney injury (AKI) following liver transplantation (LT) is associated with increased costs, morbidity, and mortality. Dexmedetomidine has known have anti-inflammatory effect and has been shown to ameliorate IRI in several organs. However, the impact of Dexmedetomidine on AKI after LT is not determined yet. Therefore, this study aims to observe the renal protective effects of Dexmedetomidine after LT.

Description

Acute kidney injury (AKI) following liver transplantation (LT) has shown a wide range of between 17% and 95% and is associated with increased costs, morbidity, and mortality. The etiology of AKI after LT is multifactorial. Among these factors, renal ischemia-reperfusion injury (IRI) caused by perioperative renal hypoperfusion is considered as one of the most important independent risk factors and recent reports have indicated that IRI is associated with an inflammatory cascade. Dexmedetomidine which is a highly selective agonist of α2-adrenergic receptors has known have anti-inflammatory effect and has been shown to ameliorate IRI in several organs. However, the impact of Dexmedetomidine on AKI after LT is not determined yet. Therefore, this study aims to observe the renal protective effects of Dexmedetomidine after LT.

Dates

Last Verified: 06/30/2019
First Submitted: 04/30/2018
Estimated Enrollment Submitted: 04/30/2018
First Posted: 05/10/2018
Last Update Submitted: 07/24/2019
Last Update Posted: 07/28/2019
Actual Study Start Date: 05/31/2018
Estimated Primary Completion Date: 12/30/2019
Estimated Study Completion Date: 12/30/2019

Condition or disease

Acute Kidney Injury
Liver Diseases

Intervention/treatment

Drug: treatment group

Phase

Phase 4

Arm Groups

ArmIntervention/treatment
No Intervention: control group
The control group was given normal saline by constant intravenous (IV) infusion at a rate of 0.4mcg/kg/hour
Active Comparator: treatment group
The treatment group was given dexmedetomidine by constant intravenous (IV) infusion at a rate of 0.4mcg/kg/hour
Drug: treatment group
The treatment group was given dexmedetomidine by constant intravenous (IV) infusion at a rate of 0.4mcg/kg/hour.

Eligibility Criteria

Ages Eligible for Study 20 Years To 20 Years
Sexes Eligible for StudyAll
Accepts Healthy VolunteersYes
Criteria

Inclusion Criteria:

- living liver transplantation recipients

Exclusion Criteria:

- preoperative renal dysfunction

- dual living donor liver transplantation

- severe cerebral artery disease

- severe cardio-pulmonary disease

Outcome

Primary Outcome Measures

1. acute kidney injury [7 days]

serum creatinine levels in postoperative 7 days

Secondary Outcome Measures

1. early graft dysfunction [7 days]

laboratory data in postoperative 7 days

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