跳至主要内容
临床试验/NCT01036932
NCT01036932Unknown不适用

To Study the Safety and Efficacy of G-CSF Therapy on the CD 34 Cell Mobilization and Outcome of Patients With ACLF

Govind Ballabh Pant Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2008年12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
入组人数
50
试验地点
1
主要终点
mobilization of CD34 cells in the peripheral blood

研究概览

简要总结

The purpose of the study is to determine whether Granulocyte Colony Stimulating factor(G-CSF) therapy is effective in the treatment of patients with Acute on chronic liver failure(ACLF). The investigators hypothesize that ACLF is a disease where severe hepatic impairment is accompanied by impaired hepatic regeneration. BMC mobilization using G-CSF therapy, or G-CSF therapy per se would increase the regenerative capacity of the liver and shall lead to clinical, biochemical and histological improvements in patients with ACLF.

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
12 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with acute hepatic insult manifesting as jaundice (Sr. Bil. ≥5 mg/dL) and coagulopathy (INR≥1.5), complicated within 4 weeks by ascites and/or encephalopathy in a patient with previously diagnosed or undiagnosed chronic liver disease.(APASL criteria)

排除标准

  • HCC or portal vein thrombosis. Refusal to participate in the study. Sepsis ( Any culture positive: blood, urine, focus of infection on Xray chest, any other obvious source of infection: UTI, SBP) Multi organ failure. Grade 3 or 4 hepatic encephalopathy.

研究组 & 干预措施

G-CSF group

Active Comparator

Patients with Acute on chronic liver failure after baseline investigations for the etiology of the acute event and the underlying chronic disease were given Granulocyte Colony Stimulating Factor therapy for a total duration of one month.

干预措施: Granulocyte Colony Stimulating Factor (Drug)

Placebo

Placebo Comparator

After baseline characterization and work up for underlying acute and chronic liver disease, patients were given placebo along with the standard therapy

干预措施: Normal Saline (Drug)

结局指标

主要结局

mobilization of CD34 cells in the peripheral blood

时间窗: 1 month

次要结局

  • clinical/ biochemical improvement in liver function profile(2 months)
  • frequency of multi-organ failure(2 months)

研究者

申办方类型
Other Gov

研究点 (1)

Loading locations...

相似试验