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临床试验/NCT00815763
NCT00815763已完成3 期

Efficacy and Safety of Ginsenoside-Rd for Acute Ischemic Stroke: A Randomized, Double-Blind, Placebo-Controlled, Phase 3, Multicenter Trial

Xijing Hospital1 个研究点 分布在 1 个国家目标入组 390 人开始时间: 2006年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
390
试验地点
1
主要终点
the modified Rankin scale

研究概览

简要总结

The purpose of this phase 3 study is to validate the efficacy and safety of ginsenoside-Rd for acute ischemic stroke.

详细描述

A phase Ⅲ randomized, double-blind, placebo-controlled, multicenter study was conducted to examine the efficacy and safety of ginsenoside-Rd in patients with acute ischemic stroke. Stroke patients were randomized equally to receive a 14-day infusion of placebo or ginsenoside-Rd 20mg. Primary end points were NIHSS scores at 15 days. Secondary end points were NIHSS scores and the Barthel index at 8 days, the Barthel index and the modified Rankin scale at 15 days and 90 days. The safety end points included serious and nonserious adverse events, laboratory values and vital signs. Analysis was by intention to treat.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • between 18 to 75 years
  • the first episode
  • from onset to admission within 72 hours
  • NIHSS scores:5~22

排除标准

  • had other intracranial pathologies (e.g., tumor, infection)
  • had a neurologic or psychiatric disease
  • had a coexisting condition that limited their life expectancy
  • had significant drug or alcohol misuse
  • had high-grade carotid artery stenosis for which surgery was planned
  • were pregnant or nursing
  • participated in a clinical trial with an investigational drug or device within the past 3 months
  • were unlikely to be available for follow-up

研究组 & 干预措施

ginsenoside-Rd 20mg

Experimental

infusion of ginsenoside-Rd 20mg once a day and continued for 14 days

干预措施: ginsenoside-Rd (Drug)

placebo

Placebo Comparator

infusion placebo (group B)once a day and continued for 14 days

干预措施: placebo (Drug)

结局指标

主要结局

the modified Rankin scale

时间窗: 90 days

次要结局

  • NIHSS scores(15 days)
  • the Barthel index(15 days)
  • the modified Rankin scale(15 days)

研究者

发起方
Xijing Hospital
申办方类型
Other

研究点 (1)

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