EUCTR2014-000096-80-LT进行中(未招募)1 期
Tenecteplase in Wake-up Ischaemic Stroke Trial (TWIST) - TWIST
niversity or Tromsø0 个研究点目标入组 500 人开始时间: 2016年11月23日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 500
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
- •Stroke symptoms on awakening that were not present before sleep
- •Clinical diagnosis of stroke with limb weakness with NIHSS score >5, or dysphasia.
- •Treatment with tenecteplase is possible within 4.5 hours of awakening
- •Written consent from the patient, non-written consent from the patient (witnessed by non-participating health care personnel), or written consent from the nearest family member.
- •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 100
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 400
排除标准
- •Age < 18 years
- •Findings on plain CT that indicate that the patient is unlikely to benifit from treatment:
- •-Infarction comprising more than >1/3 of the middle cerebral artery territory on plain CT
- •-Intracranial haemorrhage, structural brain lesions which can mimic stroke (e.g cerebral tumour)
- •Patient will be treated with intra-arterial interventions for proximal cerebral artery occlusion
- •High risk of bleeding, e.g.:
- •-Major surgery, trauma or gastrointestinal or urinary tract haemorrhage within the previous 21 days, or arterial puncture at a non-compressible site within the previous 7 days.
- •-Any known defect in coagulation, e.g. current use of vitamin K antagonist with an INR > 1.7, or other oral anticoagulant, or heparins
- •-Known defect of clotting or platelet function (but patients on antiplatelet agents can be included)
- •-Ischaemic stroke in previous 2 weeks, previous intracranial haemorrhage, or known arteriovenous malformation or aneurysm
- •Persistent blood pressure elevation (systolic =185 mmHg or diastolic =110 mmHg), despite blood pressure lowering treatment
- •Blood glucose < 3.0 or > 20.0 mmol/L
- •Childbearing potential, pregnancy, positive pregnancy test, breastfeeding
- •Other serious or life-threatening disease before the stroke: severe mental or physical disability (e.g. Mini Mental Status score < 20, or modified Rankin Scale score = 3), or life expectancy less than 12 months
- •Patient unavailability for follow-up (e.g. no fixed address)
研究者
相似试验
进行中(未招募)
1 期
Study of clot dissolving treatment for stroke that occurs during sleepEUCTR2014-000096-80-FIniversity or Tromsø500
进行中(未招募)
1 期
Study of clot dissolving treatment for stroke that occurs during sleepAcute ischaemic stroke upon awakening (wake-up stroke)EUCTR2014-000096-80-GBniversity or Tromsø500
进行中(未招募)
1 期
Study of clot dissolving treatment for stroke that occurs during sleepAcute ischaemic stroke upon awakening (wake-up stroke)MedDRA version: 20.0Level: LLTClassification code 10055221Term: Ischemic strokeSystem Organ Class: 100000004852EUCTR2014-000096-80-DKniversity or Tromsø500
已完成
3 期
Tenecteplase in Wake-up Ischaemic Stroke TrialISRCTN10601890niversity Hospital of North Norway578
Unknown
3 期
Tenecteplase in Wake-up Ischaemic Stroke TrialIschemic StrokeStroke, AcuteNCT03181360University Hospital of North Norway600
