跳至主要内容
临床试验/CTRI/2024/08/072093
CTRI/2024/08/072093招募中不适用

Evaluation of role of VEXUS score in reducing intradialytic complications in critically ill patients-A randomized controlled trial

Ninu Rose Paul1 个研究点 分布在 1 个国家目标入组 168 人开始时间: 2024年8月20日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
168
试验地点
1
主要终点
incidence of intradialytic complications between traditional and VEXUS score guided ultrafiltration goals

研究概览

简要总结

This review aims to evaluate if the VEXUS score can improve outcomes by guiding ultrafiltration in critically ill patients undergoing hemodialysis compared to conventional methods. Conventional fluid assessment in such patients is often challenging and can lead to complications from inaccurate ultrafiltration. The primary objective is to assess the incidence of intradialytic complications. Secondary objectives include comparing the number of dialysis sessions, ICU days, ventilator days, ICU mortality, and 30-day mortality between the VEXUS-guided and traditional ultrafiltration groups. The study seeks to clarify whether the VEXUS score offers a more effective approach in managing fluid removal in this vulnerable patient population.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • admission in ICU requiring dialysis.

排除标准

  • previous echocardiographic evidence of right heart dysfunction previous liver resection or transplantation liver cirrhosis pregnancy.

结局指标

主要结局

incidence of intradialytic complications between traditional and VEXUS score guided ultrafiltration goals

时间窗: 1 HOUR | 2 HOUR | 3 HOUR | 4 HOUR

次要结局

  • number of dialysis sessions required in ICU(Number of ICU days)

研究者

发起方
Ninu Rose Paul
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Ninu Rose Paul

Pushpagiri Institute of Medical Sciences and Research Centre

研究点 (1)

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