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临床试验/NCT01501097
NCT01501097Unknown不适用

A Randomized Controlled Trial on the Impact of Early Application of CRRT on the Outcomes of Burn Patients With Early Phase of Sepsis

Southwest Hospital, China1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2011年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
1
主要终点
Changes in serum cytokine concentrations and clearance

研究概览

简要总结

The purpose of this study is to determine if early application of CRRT will result in an improvement of clinical outcomes of burn patients during the early phase of sepsis

详细描述

The impact of Continuous Renal Replacement Therapy (CRRT) on the outcomes of patients with sepsis is controversial, and there is no consensus for the timing and dose of CRRT may improve the outcomes. The purpose of this prospective randomized study is to assess the effect of different CRRT intensity (25ml/kg/h or 50ml/kg/h) on the outcomes of burn patients with early phase of sepsis

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients with documented sepsis
  • clinically identified focus of infection associated with at least 2 SIRS -criteria and one or more sepsis-induced organ failures within the 24 hours -prior to inclusion
  • age 18 to 70 years
  • severe burned patients with 50% < TBSA < 85%

排除标准

  • cirrhosis child class C
  • too high APACHE II & SOFA score at admission
  • age over 70 years
  • were presence of a malignant tumor, chronic renal insufficiency (serum creatinine > 133 µmol/L), moribund state, receiving immunosuppressive therapy or receiving any kind of renal replacement therapy before randomization

研究组 & 干预措施

Control group

No Intervention

干预措施: Continuous Renal Replacement Therapy (Procedure)

early HV-crrt

Experimental

干预措施: Continuous Renal Replacement Therapy (Procedure)

结局指标

主要结局

Changes in serum cytokine concentrations and clearance

时间窗: 96 hours

0, 6, 12 , 24, 48, 96 hours post CRRT

次要结局

  • 28 and 90 days survival(90 days)

研究者

发起方
Southwest Hospital, China
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhiqiang Yuan

Associate Professor

Southwest Hospital, China

研究点 (1)

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