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临床试验/JPRN-jRCT2080221447
JPRN-jRCT2080221447未知3 期

AJH801 Phase III Comparative Clinical Study in individuals with essential hypertension

Ajinomoto Pharmaceuticals Co., Ltd.0 个研究点目标入组 600 人开始时间: 2011年4月27日最近更新:
适应症

试验速览

阶段
3 期
发起方
入组人数
600

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • In observation period
  • -140 mmHg < the sitting SBP at trough < 199 mmHg
  • - 90 mmHg < the sitting DBP at trough < 114 mmHg
  • At the end of observation period
  • -150 mmHg < the sitting SBP at trough < 199 mmHg
  • - 95 mmHg < the sitting DBP at trough < 114 mmHg
  • The difference in observation period
  • -The difference between the sitting trough SBP at 2 points in observation period is within 30 mmHg.
  • -The difference between the sitting trough DBP at 2 points in observation period is within 15 mmHg.

排除标准

  • - Females who are pregnant, are breast-feeding, are potentially pregnant, are planning to be pregnant during the study period
  • - Patients with secondary hypertension, or suspected of having secondary hypertension
  • - Significant heart, renal, hepatic diseases or significant cerebrovascular disorder

研究者

发起方
Ajinomoto Pharmaceuticals Co., Ltd.

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