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临床试验/NL-OMON54804
NL-OMON54804招募中3 期

Triple therapy prevention of Recurrent Intracerebral Disease EveNts Trial - TRIDENT

The George Institute for Global Health - Australia0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
25

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
18 至 99(—)

入选标准

  • 1. Adults (>=18 years) with a history stroke due to primary intracerebral
  • haemorrhage (ICH) confirmed by brain imaging, 2. Clinically stable, as judged
  • by investigator, 3. Two resting systolic BP (SBP) levels, measured 5 minutes
  • apart in the range 130-160mmHg recorded in a seated position., 4. Provision of
  • written informed consent.

排除标准

  • 1. Taking an ACE inhibitor antihypertensive drug that cannot be switched to any
  • of the following alternatives:, - telmisartan 20 or 40mg, amlodipine 2.5 or
  • 5mg, indapamide 1.25, or;, - an equivalent class (angiotensin receptor blocker,
  • calcium channel blocker, or thiazide-like diuretic), or;, - a beta-blocker, 2.
  • Contraindication to any of the study medications, in the context of currently
  • prescribed BP lowering medication, 3. Unlikely/unable to complete the study
  • procedures and/or follow-up, 4. Females of child bearing age and capability,
  • who are pregnant or breast-feeding, or those not using adequate contraception,
  • 5. Any condition that in the opinion of the responsible physician or
  • investigator that renders the patient unsuitable for the study (e.g. severe
  • disability (ie modified Rankin Scale [mRS] score of 4-5] or significant memory
  • or behavioural disorder or hyperkalaemia and/or hyponatremia, defined by local
  • lab criteria)

研究者

发起方
The George Institute for Global Health - Australia

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