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临床试验/NCT04892745
NCT04892745已完成不适用

Impact of Hemodialysis on Cutaneo-muscular Electrical Impedance

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2021年9月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
1
主要终点
Electrical parameters of subcutaneous impedancemetry

研究概览

简要总结

The primary objective of this pilot study aims to describe the modifications of subcutaneous impedancemetry induced by dialysis.

As secondary objectives, the study aims to 1) describe the modifications of cutaneo-muscular impedancemetry induced by dialysis. 2) describe the relationship between modifications of subcutaneous impedancemetry induced by dialysis and - technical conditions of dialysis; - volemic parameters of dialysis; - evolution of liquid compartments in organism during dialysis; - volemic events or neuromuscular events. 3) describe the relationship between modifications of cutaneo-muscular impedancemetry induced by dialysis and 1) describe the modifications of cutaneo-muscular impedance induced by dialysis. 2) describe the relationship between modifications of subcutaneous impedancemetry induced by dialysis and - technical conditions of dialysis; - volemic parameters of dialysis; - evolution of liquid compartments in organism during dialysis; - volemic events or neuromuscular events.

详细描述

The study will be realized in dialysis facility of Ambroise Paré hospital, APHP. The duration of enrollment of subjects will be 3 months, each enrolled patient will has 2 or 3 week's follow-up.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient ⩾ 18 years;
  • Patient undergoing chronic dialysis in hemodialysis facility of Ambroise Paré hospital;
  • Patient has been informed and given no-opposition for participating to the study.

排除标准

  • Patient with a pacemaker or an implantable cardioverter defibrillator;
  • Patient under guardianship or curatorship;
  • Foreign patient under french AME scheme.

结局指标

主要结局

Electrical parameters of subcutaneous impedancemetry

时间窗: at the end of study, up to 4 months

Electrical parameter extracellular resistance (Re) will be assessed.

次要结局

  • Whole body impedancemetry assessement(at the end of study, up to 4 months)
  • Cutaneo-muscular impedancemetry assessement(at the end of study, up to 4 months)
  • Incidence of volemic or neuromuscular events(at the end of study, up to 4 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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