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
相似试验
进行中(未招募)
1 期
Triple therapy prevention of Recurrent Intracerebral Disease EveNts Trial (TRIDENT)Patients with a history of acute stroke due to Intracranial Haemorrhage with mild to moderately high blood pressure.MedDRA version: 21.1Level: PTClassification code 10019016Term: Haemorrhagic strokeSystem Organ Class: 10029205 - Nervous system disordersEUCTR2016-003724-23-GBThe George Institute for Global Health, University of New South Wales1,500
招募中
3 期
Triple therapy prevention of Recurrent Intracerebral Disease EveNts Trialbrain haemorrhageIntracerebral haemorrhage1000796310047075NL-OMON54804The George Institute for Global Health - Australia25
已完成
3 期
Triple Therapy Prevention of Recurrent Intracerebral Disease EveNts TrialIntracerebral Haemorrhage (ICH)HypertensionNCT02699645The George Institute1,671
终止
3 期
Triple Therapy Prevention of Recurrent Intracerebral Disease EveNts Trial (TRIDENT) Cognitive Sub-StudyCognitive DeclineIntracerebral HemorrhageDementia, VascularCerebral Small Vessel DiseasesStroke HemorrhagicHypertensionNCT03785067The George Institute1
终止
不适用
Triple Therapy Prevention of Recurrent Intracerebral Disease EveNts Trial Magnetic Resonance Imaging Sub-studyCerebral Small Vessel DiseasesIntracerebral HemorrhageStrokeHypertensionVascular DementiaNCT03783754The George Institute4
