Clinical Trials Directory

Trials / Unknown

UnknownNCT03522688

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

Impact of Dexmedetomidine on Acute Kidney Injury Following Living Donor Liver Transplantation: A Randomized Controlled Study

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
214 (actual)
Sponsor
Asan Medical Center · Academic / Other
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Acute kidney injury (AKI) following liver transplantation (LT) is associated with increased costs, morbidity, and mortality. Dexmedetomidine has known to 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.

Detailed description

Acute kidney injury (AKI) following liver transplantation (LT) has shown a wide range of incidence 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.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidineThe treatment group was given dexmedetomidine by constant intravenous (IV) infusion at a rate of 0.4mcg/kg/hour.
DRUGNormal salineThe control group was given normal saline by constant intravenous (IV) infusion at a rate of 0.4mcg/kg/hour

Timeline

Start date
2017-07-11
Primary completion
2023-07-14
Completion
2024-07-07
First posted
2018-05-11
Last updated
2023-07-17

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03522688. Inclusion in this directory is not an endorsement.