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临床试验/NCT02756741
NCT02756741已完成不适用

Assessment of Cytokine Profile in an Open Labeled Randomized Controlled Trial of Standard Dose vs. Once a Day Intravenous Albumin in Patients With Spontaneous Bacterial Peritonitis

All India Institute of Medical Sciences, New Delhi0 个研究点目标入组 40 人开始时间: 2014年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
主要终点
Change in neutrophils/mm in ascitic fluid

研究概览

简要总结

The standard recommended management of spontaneous bacterial peritonitis (SBP) includes a third-generation cephalosporin (cefotaxime or ceftriaxone) and high dose albumin (1.5g/kg on day 1 and 1g/kg on day 3). The major drawback of the current recommendations is the high price of albumin. In the current randomized control trial investigators compared the effect of standard recommended dose of albumin (1.5g/kg on day 1 and 1g/kg on day 3) vs. low dose (20g/d for 5 days) on the resolution of SBP and subsequent cytokine changes in ascitic fluid and blood.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

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

  • Diagnosis of SBP
  • Age > 18 years
  • Consent to participate in the trial

排除标准

  • Secondary peritonitis
  • Malignancies including HCC

研究组 & 干预措施

STANDARD DOSE

Active Comparator

Albumin 1.5gm/kg on day 1 and 1gm/kg on day 3

干预措施: ALBUMIN (Drug)

LOW DOSE

Placebo Comparator

Albumin 20g/d for 5 days

干预措施: ALBUMIN (Drug)

结局指标

主要结局

Change in neutrophils/mm in ascitic fluid

时间窗: 3 days

Change in IL-6, IL-1, TNF in ascitic fluid and serum between the two groups

时间窗: 5 days

次要结局

  • Survival in days at the end of therapy(5 days)
  • Differences in frequency of sepsis, renal failure and other organ failures between the two groups(5 days)

研究者

发起方
All India Institute of Medical Sciences, New Delhi
申办方类型
Other
责任方
Principal Investigator
主要研究者

Subrat Kumar Acharya

Professor and Head, Department of Gastroenterology

All India Institute of Medical Sciences, New Delhi

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