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临床试验/NCT03506893
NCT03506893招募中不适用

Medical-economic Evaluation of the Care of Refractory Ascites by Implantation of Alfapump® Device in Cirrhotic Patients

University Hospital, Grenoble10 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2018年7月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
90
试验地点
10
主要终点
Evaluation of medical-economic impact at 1 year of 2 strategies: implantation of Alfapump® device versus repeated evacuating paracentesis (reference treatment) in cirrhotic patients with refractory ascites without programmed liver transplantation.

研究概览

简要总结

The hypothesis is that the Alfapump® strategy would be more effective in terms of QALYs generated , and that the cost of Alfapump® device and its implantation will be totally or partially offset by the reduction in the number of evacuating parentheses performed and the reduction in the number of complications in patients with refractory ascites awaiting liver transplantation or not. On the other hand, given the difference in the clinical profiles of these two populations (whether or not they are awaiting transplantation), these two populations will be study separately

Evaluation of the medical-economic impact at 1 year of the two therapeutic strategies: implantation of Alfapump® versus repeated evacuating paracentesis in cirrhotic patients with refractory ascites without scheduled liver transplantation.

详细描述

Refractory ascites is one of the complications associated with portal hypertension in the cirrhotic patient. To date, its treatment consists of evacuating punctures, performed in day hospitalisation, whose frequency is adapted to the rate of ascites synthetis. Paracentesis, which does not affect the mechanisms of ascites formation, contributes to protein catabolism and undernutrition. They also have an inconvenience linked to the gesture, making frequent hospital stays necessary. For all these reasons, the patient's quality of life is diminished. The Alfapump® system is a new method for the treatment of refractory ascites. It is a completely internalized medical device, implanted under the skin, which mobilizes ascites from the peritoneal cavity to the bladder, where ascites is eliminated by urinary tract.

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
否

入选标准

  • •Patient with refractory ascites who has had a minimum of 5 paracentesis in the last 3 months.
  • •Patient with an estimated life expectancy of at least 6 months on the day of inclusion.
  • •Patient with contraindication to the application of a TIPS or who has expressed a refusal of the procedure or a non-functional TIPS
  • •Patient affiliated with or in receipt of social security
  • •Informed and written consent signed by the patient.

排除标准

  • •Local or systemic infection in the month preceding the procedure
  • •Hepatocellular carcinoma with palliative care
  • •MELD Score > 18
  • •Child Pugh C Score > 10
  • •Creatinine Clearance < 50 ml/mn
  • •Digestive hemorrhage or episode of hepatic encephalopathy within two weeks prior to device insertion
  • •Contraindication to general anesthesia
  • •Contraindication to implant surgery of the device:
  • •Obstructive urological impairment
  • •Partitioning of ascites
  • •Coagulopathy
  • •Persons referred to in Articles L1121-5 to L1121-8 of the CSP (corresponding to all protected persons: pregnant woman, parturient, breastfeeding mother, person deprived of liberty by judicial or administrative decision, person subject to a legal protection measure).
  • •Patient currently participating in other clinical research or who participated in a clinical trial within one month prior to inclusion.

研究组 & 干预措施

Alphapump

Experimental

Alfapump® device implantation under general anesthesia (30-45 minutes)

干预措施: Alphapump (Device)

Ascites puncture

Active Comparator

Iterative paracentesis compensated for by albumin infusions in ambulatory care.

干预措施: Ascites puncture (Procedure)

结局指标

主要结局

Evaluation of medical-economic impact at 1 year of 2 strategies: implantation of Alfapump® device versus repeated evacuating paracentesis (reference treatment) in cirrhotic patients with refractory ascites without programmed liver transplantation.

时间窗: 1 year

Incremental cost-utility ratio (ICER) from societal perspective.

次要结局

  • Evaluation of the economic impact at 6 and 12 months of Alfapump® versus repeated evacuating paracentesis in cirrhotic patients with refractory ascites WITH programmed liver transplantation.(6 months and 1 year)
  • Evaluation of the clinical impact at 2 years of Alfapump® versus repeated evacuating paracentesis (prospective observational study).(2 years)
  • Evaluation of the economic impact at 2 years of Alfapump® versus repeated evacuating paracentesis (prospective observational study).(2 years)
  • Budget impact Analysis from the point of view of French health insurance, at 3 and 5 years.(3 and 5 years)
  • Comparison of the clinical impact at 6 and 12 months of Alfapump® versus repeated evacuating paracentesis in cirrhotic patients with refractory ascites WITHOUT programmed liver transplantation.(6 months and 1 year)
  • Evaluation of the clinical impact at 6 and 12 months of Alfapump® versus repeated evacuating paracentesis in cirrhotic patients with refractory ascites WITH programmed liver transplantation.(6 months and 1 year)

研究者

发起方
University Hospital, Grenoble
申办方类型
Other
责任方
Sponsor

研究点 (10)

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