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临床试验/TCTR20220622004
TCTR20220622004已完成4 期

A Randomized Controlled Trial Comparing Blood Pressure Reduction in Hyperacute Phase of Spontaneous Intracerebral Hemorrhage by Continuous Nicardipine Infusion with or without a Preceding Nicardipine Bolus dose

avamindradhiraj University0 个研究点目标入组 62 人开始时间: 2022年6月22日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
62

研究概览

简要总结

There were no significant differences in baseline SBP between the two groups, but the bolus group achieved the target SBP of 180 mmHg more rapidly. No patients in either group experienced neurological deterioration during the first hour of treatment, and the infusion dosages of Nicardipine at 1 hour were not statistically significantly different in both groups.

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 1. Spontaneous intracerebral hemorrhage
  • 2. 18-year-old or more
  • 3. Systolic blood pressure 180 mmHg or more
  • 4. GCS more than 5

排除标准

  • 1. pregnancy
  • 2. intraventricular hemorrhage, subarachnoid hemorrhage
  • 3. Hematoma volume greater than 60 milliliters
  • 4. onset more than 6 hours
  • 5. refer in
  • 6. allergic to Nicardipine
  • 7. unobtainable a consent form

研究者

发起方
avamindradhiraj University

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