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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04317222
Other study ID # LTeCRRT-P1
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 1, 2020
Est. completion date August 31, 2022

Study information

Verified date March 2020
Source Third Affiliated Hospital, Sun Yat-Sen University
Contact Huimin Yi, doctor
Phone 18922102510
Email ylhmin@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pretransplant hepatoencephalopathy (HE) markedly impacts recipient outcomes after liver transplantation. Intraoperative CRRT showed benefits but feasibility was much concerned. This study aims to observe the effect on consciousness recovery when initiating CRRT early in the post-transplant period in recipients with ACLF and overt HE.


Description:

Hepatoencephalopathy (HE) is a common severe decompensation in end stage liver diseases and resulted to the need of liver transplantation (LT). Pretransplant HE markedly impacts recipient outcomes after liver transplantation. HE in acute on chronic liver failure (ACLF) is categorized to type C HE. Hyperammonemia and systemic inflammation have been reported to contribute its development. Continuous renal replacement therapy (CRRT) has been shown great benefits in ACLF patients with HE. Intraoperative CRRT in LT also showed benefits but feasibility was much concerned. Our preliminary retrospective data showed that early CRRT (eCRRT) after LT reduced consciousness recovery time, ventilation days and post-transplant infection rate.

This open label, parallel randomized trial will observe the effect on consciousness recovery when initiating CRRT early (eCRRT) in the post-transplant period in recipients with ACLF and overt HE.

The CRRT safety and ventilation days, infection, mortality and ICU stay will also be measured.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 250
Est. completion date August 31, 2022
Est. primary completion date May 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: Liver transplant recipients who meet all of the following criteria will be enrolled

1. Pre transplant liver failure: Total bilirubin over 171µmol/L and prothrombin activity (PTA)<40%;

2. Overt hepatic encephalopathy(HE): Grade II or higher HE according West Haven classification;

3. HE associated with acute liver failure (Type A) or cirrhosis complicated with portal hypertension and/or portal systemic shunts (Type C)

Exclusion Criteria:

1. Patients with a previous history of kidney-related diseases and glomerular filtration rate <30 millilitre per minute;

2. Patients with acute renal failure need CRRT before transplantation;

3. Patients newly developed acute renal failure need CRRT at the time of randomization;

4. Retransplantation or multiple-organs transplantation;

5. Any ischemic or hemorrhagic stroke co-morbidity;

6. Hemodynamic instability requiring fluid resuscitation or very high dose of vasopressors;

7. Extremely moribund patients with an expected life expectancy of less than 24 hours.

Study Design


Intervention

Device:
eCRRT
eCRRT was define as: Initiated within the first 24 post-transplant hours; High volume (35-50ml/kg) hemofiltration; Continuous at least 12 hours per day for 3 days; Standard treatment

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Third Affiliated Hospital, Sun Yat-Sen University

References & Publications (1)

Yi H, Lv H, An Y, Yi X, Wei X, Chen G (2015) Early Continuous Blood Purification(CBP) Deceased the Incidence of Pulmonary Infection after Liver Transplantation in Severe End-Stage-Liver-Disease Recipients With Hepatic Encephalopathy. Transplantation 99:20

Outcome

Type Measure Description Time frame Safety issue
Primary Consciousness recovery time The period from post-transplant immediate to the time when the patient have the first spontaneous eye opening and proper motor response to commands. From the immediate to 30 days after liver transplantation
Primary Adverse events Any adverse event which probable related with CRRT From the immediate to 7 days after liver transplantation (CRRT therapy period)
Secondary Invasive ventilation days The time period when patients breath with ventilator through artificial airway From the immediate to 30 days after liver transplantation
Secondary ICU stay (days) The time period from transplantation to first ICU discharge up to one year
Secondary Reintubation rate Reintubation after the first extubation following liver transplantation From the immediate to 30 days after liver transplantation
Secondary 90 days mortality All cause mortality From the immediate to 90 days after liver transplantation
Secondary Infection rate Any diagnosed infection after transplantation in 30 days From the immediate to 30 days after liver transplantation
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