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临床试验/NCT06989892
NCT06989892招募中不适用

Comparing Super High-flux and High-flux Dialyzer Performance Among Hemodialysis Patient With Sepsis : a Randomized Control Trial

Navamindradhiraj University2 个研究点 分布在 1 个国家目标入组 202 人开始时间: 2024年7月25日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
202
试验地点
2
主要终点
Comparing the reduction of all cause death at 28 days

研究概览

简要总结

Comparing the efficacy of superhigh-flux dialyzer with high-flux dialyzer in ESKD patient who have sepsis to improve mortality and sepsis outcome, an open label randomized control trial.

详细描述

Sepsis in people who have ESKD is the risk of developing poor outcome. Cytokines play a role in the process of sepsis and cause the worsening clinical outcome despite definitive antibiotic treatment. Superhigh-flux dialyzer has a larger molecular weight cut off (MWCO) clearance, include cytokine, could contribute to improved sepsis management in individuals with ESKD. This study is conducted to prove the efficacy of super high-flux dialyzer comparing with high-flux dialyzer in case of mortality reduction for regular hemodialysis ESKD patients.

Method This study is an open label single center randomized control trial. We randomized ESKD patients who have sepsis condition with high interleukin-6 (IL-6 > 50 pg/ml).

The participants were allocated to super high-flux dialyzer group and high flux dialyzer group, stratified with diabetes, vascular access, and septic shock.

We excluded; patient who needed dialysis with continuous kidney replacement therapy, vulnerable patient, include pregnant woman, patient who closed and patient who expected to pass away within the 24 hours. We aim to enroll total 202 participants; divided equally in each arm. According to our protocol, non reused super high-flux dialyzer and high-flux dialyzer are used in the same assigned patient in first week without crossing over. The standard of care of sepsis and antibiotic are provided in both groups without intervening of researcher and our protocol. The primary endpoint is 28 days of mortality. The secondary outcome include cardiovascular death, rate reduction of IL-6 after dialysis, days of hospitalization, ventilator free days and complication of dialysis are also monitored.

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
Single (Participant)

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

  • ESKD patients who have sepsis condition with high interleukin-6 (IL-6 > 50 pg/ml)

排除标准

  • Patients who needed dialysis with continuous kidney replacement therapy, vulnerable patient, include pregnant woman, patient who expected to pass away within the 24 hours.
  • Patients who have the history of allergic dialyzer reaction to dialyzer which used in this trial.

结局指标

主要结局

Comparing the reduction of all cause death at 28 days

时间窗: 28 days

Comparing the efficacy to reduce all cause death at 28 days between Super High-flux dialyzer with High-flux dialyzer in ESKD with sepsis

次要结局

  • Comparing the difference of blood level of IL-6, ESR, CRP and albumin, before and after of the first dialysis session, in each group.(7 days)
  • The duration of inotrope weaning(14 days)
  • The duration of hospitalization(28 days)
  • The incidence of intradialytic hypotension(28 days)
  • Ventilator free days(28 days)
  • The incidence rate of complication of dialyzer in each group(28 days)
  • The adequacy profile of dialysis in both groups(7 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Punnawit Laungchuaychok

Dr.

Navamindradhiraj University

研究点 (2)

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