跳至主要内容
临床试验/NCT06129617
NCT06129617招募中不适用

Prospective Randomized Controlled Trial for Protein-bound Toxins Removal With Intermittent ADVOS vs. Hemodialysis Treatment in Non-intensive Care Patients With Pre-existing Liver Dysfunction and Indication for Extracorporeal Renal Support. The ADVOMITTENT Study

University Medical Center Mainz2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2023年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
14
试验地点
2
主要终点
course of total bilirubin in patients blood

研究概览

简要总结

In the planned randomized controlled prospective pilot study, we aim to evaluate ADVOS compared with conventional hemodialysis regarding the elimination of protein-bound toxins in patients with therapy-refractory hepatorenal syndrome.

The study will be performed in a regular non-ICU ward with a large experience in the use of the ADVOS therapy.

详细描述

Acute on chronic liver failure (ACLF) is a syndrome in patients with liver cirrhosis characterized by acute hepatic decompensation (i.e., jaundice, ascites, hepatic encephalopathy, bacterial infection, or gastrointestinal bleeding) and single or multi-organ failure, resulting in increased mortality. The European Association for the Study of the Liver (EASL) has established the Chronic Liver Failure (CLIF) consortium, which has developed a score for risk stratification and prognosis estimation, the CLIF-C ACLF score. Based on the CANONIC study, the CLIF consortium has developed a simplified CLIF Consortium Organ Failure Score (CLIF-C OFs), which includes liver, kidney, and lung function, hepatic encephalopathy, coagulation, and hemodynamics. Considering two other mortality factors (age and leukocyte count), the CLIF-C ACLF score was defined. The score has a higher predictive value for 28- and 90-day mortality than the Model of End Stage Liver Disease (MELD), MELD-Na, or Child-Turcotte-Pugh score.

Therapeutic options are limited and aim to address specific organ complications. In most cases, due to progressive renal insufficiency as part of hepatorenal syndrome, renal replacement therapy is if indicated. The only potential cure is liver transplantation.

There is some evidence that extracorporeal liver support can help a patient until liver transplantation or restoration of organ function. The Advanced Organ Support (ADVOS) system (ADVITOS GmbH, Munich, Germany) is an albumin-based advanced hemodialysis procedure, which can support the liver. The principles of conventional renal replacement therapy for the elimination of water-soluble substances are combined with the elimination of protein-bound substances by recirculating a dialysate containing 200 ml of human albumin. This procedure is typically used as continuous treatment in an intensive care setting. However, the investigators have already investigated the possibility of ADVOS as an intermittent procedure in patients with ACLF on a regular ward in a retrospective study.

To the best of knowledge of the investigators, there are currently no randomized studies comparing the elimination of protein-bound toxins between ADVOS and hemodialysis. Nevertheless, based on the investigators clinical experience, the investigators hypothesize that treatment with ADVOS may confer advantages over hemodialysis. Therefore, the objective of this study is to assess the effectiveness of ADVOS in comparison to hemodialysis for the treatment of patients with therapy-refractory hepatorenal syndrome.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Capacity of the patient to give consent
  • Pre-existing liver disease in the sense of an ACLF with HRS
  • Age >18 years
  • Patient of the University Medical Center Mainz
  • Bilirubin level ≥ 4 mg/dl
  • Indication for renal replacement procedure is based on STARRT-AKI criteria (serum potassium ≥ 6 mmol/l in two independent blood samples; serum pH of 7.2 or less or serum bicarbonate of 12 mmol/l or less; respiratory failure secondary to volume excess)

排除标准

  • Age < 18 years
  • Pregnancy
  • Contraindications for ADVOS therapy
  • Already started renal replacement therapy
  • Contraindication for citrate anticoagulation
  • Use of vasopressors and MAD ≤ 50 mmHg.
  • Terminal cancer

结局指标

主要结局

course of total bilirubin in patients blood

时间窗: Within 6 hours before first treatment and within 2 hours after every treatment session

measurement of concentration of total bilirubin in serum of patients in mg/dl

次要结局

  • number of days in hospital during the intervention(admission in our department till discharge from our deparment)
  • evaluation of safety of ADVOS versus hemodialysis(during the five interventions)
  • course of albumin(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of base excess(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of standard bicarbonat concentration(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of potassium(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of uremia toxins in patients blood(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of bile acids(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • Quality of life raised in a standardized questionnaire(baseline before intervention and on days 28, 90, 180)
  • course of INR(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of MELD(Within 6 hours before first treatment and within 2 hours after 5 treatments)
  • course of pCO2(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of pO2(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of ionised calcium(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • mortality(28, 90 and 180 days.)
  • course of pH(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of bilirubin(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of kidney function(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of CLIF-C ACLF score(Within 6 hours before first treatment and within 2 hours after 5 treatments)
  • course of sodium(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • elimination of blood urea nitrogen(Within 6 hours before first treatment and within 2 hours after every treatment session)
  • course of hepatic encephalopathy(Within 6 hours before first treatment and within 2 hours after every treatment session)

研究者

发起方
University Medical Center Mainz
申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Dr. Julia Weinmann-Menke

Head of nephrology and kidney transplantation

University Medical Center Mainz

研究点 (2)

Loading locations...

相似试验

Intermittent ADVOS vs. Hemodialysis in Non-intensive... | 临床试验