跳至主要内容
临床试验/NCT00327704
NCT00327704已完成4 期

Multicenter, Prospective, Randomized, Controlled Open Study Albumin 20% Versus Saline

Laboratoire français de Fractionnement et de Biotechnologies1 个研究点 分布在 1 个国家目标入组 794 人开始时间: 2006年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
794
试验地点
1
主要终点
Mortality, any cause, during the 28 day period after randomization

研究概览

简要总结

Objective: To determine whether the early administration of albumin as an expander and antioxidant would improve survival on the 28th day for septic shock patients.

Design: Prospective, multicenter, randomized, controlled versus saline, stratified on nosocomial infection and center.

Setting: 27 Intensive Care Units (ICU) in France

Coordinator: Pr J.P. Mira and Dr J. Charpentier - Cochin Hospital- Paris

Patients: 800 patients could be included during the first 6 hours of their septic shock.

详细描述

The primary outcome: Mortality during the 28 day period after randomization. The secondary outcomes: Evaluation of SOFA score, ventilator-free days, dialysis free days, catecholamine free days, days of hospitalisation, incidence of nosocomial infections.

The albuminemia of all patients is requested before the treatment until Day 4 post treatment.

The treatment is: Vialebex 20% 100ml every 8 hours during 3 days versus saline 100ml every 8 hours during 3 days.

The first patient will be in July 2006, the last patient expected is on July 2009.

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

入选标准

  • Over 18 years old
  • Septic shock < 6 hours
  • Agreement of patients

排除标准

  • Allergy to albumin
  • Weight > 120 kg
  • Non septic shock
  • Cirrhosis
  • Albumin perfusion 48 hours before randomization
  • Pregnant women
  • Cardiac dysfunction New York Heart Association (NYHA) 3 or 4
  • Patients with therapeutic limitation

研究组 & 干预措施

Albumin

Active Comparator

干预措施: albumin (Drug)

Saline

Placebo Comparator

干预措施: saline (Drug)

结局指标

主要结局

Mortality, any cause, during the 28 day period after randomization

时间窗: day 28

次要结局

  • Evaluation of sequential organ failure assessment (SOFA) score(ICU period)
  • catecholamine free days(day 28)
  • incidence of nosocomial infection(ICU period)
  • mortality at 90 days(day 90)
  • length of ICU hospitalisation(ICU discharge)
  • length of total hospitalisation(hospital discharge)

研究者

发起方
Laboratoire français de Fractionnement et de Biotechnologies
申办方类型
Industry

研究点 (1)

Loading locations...

相似试验