跳至主要内容
临床试验/EUCTR2016-003724-23-NL
EUCTR2016-003724-23-NL进行中(未招募)1 期

Triple therapy prevention of Recurrent Intracerebral Disease EveNts Trial - TRIDENT

The George Institute for Global Health, University of New South Wales0 个研究点目标入组 4,200 人开始时间: 2017年10月31日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
4,200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Adults (=18 years) up to 6 months after symptom onset of 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. No major contraindications to any of the study treatments.
  • 5. Provision of written informed consent.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 2000
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 2200

排除标准

  • 1. Taking an ACE inhibitor antihypertensive drug that cannot be switched to any of the following alternative medications:
  • o telmisartan 20 or 40mg, amlodipine 2.5 or 5mg, indapamide 1.25 or 2.5mg, or;
  • o an equivalent class (angiotensin receptor blocker, calcium channel blocker, or thiazide-like diuretic), or;
  • o 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. Significant hyperkalaemia and/or hyponatriemia, in the opinion of the responsible physician.
  • 6. Estimated glomerular filtration rate (eGRF) < 30 mL/min.
  • 7. Severe hepatic impairment (ALT or AST > 3x the upper limit of normal).
  • 8. Any other 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).

研究者

发起方
The George Institute for Global Health, University of New South Wales

相似试验