跳至主要内容
临床试验/JPRN-jRCT1062230034
JPRN-jRCT1062230034招募中Unknown

A single-center open-label crossover study of the clinical utility and safety of the BV-UFC system of the DCS-200Si dialysis monitor

Hamada Shintaro0 个研究点目标入组 20 人开始时间: 2023年7月4日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 90age old(—)
性别
All

入选标准

  • (1) Patients who give written consent to participate in this study of their own free will.
  • (2)Hemodialysis patients who are outpatients or inpatients undergoing hemodialysis (regardless of the underlying disease)
  • (3)Patients who are between 20 and 90 years old (regardless of gender) at the time of consent
  • (4)Patients who can be get a blood flow rate of 200 mL/min or more by vascular access
  • (5)Patients who have been receiving hemodialysis for at least 3 months at the time of participation in this study

排除标准

  • Of those who meet the above selection criteria, those who meet any of the following criteria shall not be eligible for enrollment.
  • (1) Patients participating in other clinical research or clinical trials
  • (2)Those who are pregnant
  • (3)Patients who have vascular access recirculation
  • (4) Patients who are deemed by the investigator to be inappropriate to participate in the study.

研究者

发起方
Hamada Shintaro

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