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临床试验/NCT04445558
NCT04445558已完成不适用

Study of Two Modalities of Dialysis and Nutrition on the Nutritional Status of Malnourished Chronic End-stage Renal Disease Patients Dependent on Intradialytic Parenteral Nutrition

GCS Ramsay Santé pour l'Enseignement et la Recherche1 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2020年7月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
11
试验地点
1
主要终点
Evolution of the nutritional status

研究概览

简要总结

Describe the impact of dialysis by high permeability and adsorbent membrane (PEPA®) associated with oral nutritional supplementation on the nutritional status of malnourished chronic end-stage renal disease patients dependent on intradialytic parenteral nutrition.

详细描述

The study proposes to compare the nutritional state after 6 months of dialysis with standard membrane associated with intradialytic parenteral nutrition (retrospective phase) with the nutritional state after 6 months of dialysis with high permeability membrane associated with oral nutritional supplementation (prospective phase).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Supportive Care
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

  • Patient with renal failure, on hemodialysis for at least 12 months;
  • Hemodialysis patient in 3 weekly sessions on a device with a standard permeability membrane (polysulfone, polyethersulfone or polyartylethersulfone type);
  • Malnourished patient, on intradialytic parenteral nutrition for at least 6 months;
  • Patient who may benefit, according to the doctor, from a change in dialysis and nutrition strategy:
  • Patient who signed an informed consent form to participate in the study

排除标准

  • Known allergy to PEPA® ;
  • Protected patient (under legal protection, or deprived of liberty by judicial or administrative decision);
  • Patient with a chronic infection in progress;
  • Patient with life expectancy <6 months according to the investigator;
  • Inability to understand information related to the study (linguistic, psychological, cognitive reason, etc.);
  • Pregnant woman or likely to be (of childbearing age, without effective contraception) or breastfeeding;
  • Patient participating in another clinical trial, or in a period of exclusion from another clinical trial;
  • Patient not benefiting from a social security scheme.

结局指标

主要结局

Evolution of the nutritional status

时间窗: Month 6

The main endpoint is the evolution between M0 and M6 of the nutritional status measured by the serum albumin level.

次要结局

  • Appearance of adverse events(Month 6)
  • Measure of the Quality of life(Month 6)
  • Evolution of nutritional assessment(Month 6)

研究者

发起方
GCS Ramsay Santé pour l'Enseignement et la Recherche
申办方类型
Other
责任方
Sponsor

研究点 (1)

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