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临床试验/EUCTR2015-004505-16-IE
EUCTR2015-004505-16-IE进行中(未招募)1 期

CONVINCE - (COlchicine for preventioN of Vascular Inflammation in Non- CardioEmbolic stroke) – a randomised clinical trial of low-dose colchicinefor secondary prevention after stroke

niversity College Dublin0 个研究点目标入组 3,154 人开始时间: 2016年6月7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
3,154

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

  • To be eligible for inclusion, each subject must meet each of the following
  • criteria at the screening assessment and baseline visit.
  • 1. Written informed consent consistent with ICH-GCP guidelines and
  • local laws signed prior to all trial-related procedures.
  • 2. Age 40 years or greater.
  • 3. Patient has had either;-
  • An ischaemic stroke without major disability (modified Rankin score 3 or
  • less)(Clarification - retinal infarction due to retinal artery occlusion is
  • A high risk TIA*
  • A brain CT or MRI has excluded primary intracranial haemorrhage
  • The stroke/TIA has occurred more than 72 hours before randomisation
  • AND no more than 28 days prior to randomisation
  • * High-risk TIA is defined as transient focal neurological symptoms of
  • presumed vascular cause with, in addition, one or more of the following
  • (a) ABCD2 score 4 or more, with motor or speech symptoms (dysarthria
  • or dysphasia)
  • (b) DWI hyperintensity on acute MRI
  • (c) Stenosis (lumen narrowing of 50% or greater on ultrasound, MRA,
  • CTA, or invasive angiography) of the internal cartoid, vertebral, middle
  • cerebral, anterior cerebral, or basilar artery in the arterial territory
  • consistent with symptoms.
  • 4. Qualifying stroke/TIA probably caused by large artery stenosis, small
  • artery occlusion (lacunar stroke), or cryptogenic embolism, with cardiac
  • embolism or other defined stroke mechanism deemed unlikely, in the
  • opinion of the treating physician.
  • 5. eGFR greater than or equal to 50 ml/min.
  • 6. In the opinion of the treating physician, patient is medically-stable,
  • capable of participating in a randomised trial, and willing to attend
  • follow-up.
  • 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 1125
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 2029

排除标准

  • 1.Stroke/TIA, probably caused by identified atrial fibrillation
  • (permanent or paroxysmal), in the opinion of the treating physician.
  • 2.Stroke/TIA probably caused by other identified cardiac source (intracardiac thrombus, endocarditis, metallic heart valve, low ejection
  • fraction <30%),
  • 3.Stroke/TIA caused by dissection, endocarditis, paradoxical
  • embolism, drug use, venous thrombosis, carotid or cardiac surgery,
  • hypercoagulability states, migraine, or inherited cerebrovascular
  • 4.History of myopathy or myalgias with raised creatine kinase (CK) on
  • statin therapy.
  • 5.Blood dyscrasia (haemoglobin<10g/dL,platelet count <150 x109/L,
  • white cell count <4 x109/L)
  • 6.Impaired hepatic function (transaminases ALT and/or AST greater
  • than twice upper limit of normal)
  • 7.Concurrent treatment with colchicine contraindicated drugs:-
  • CYP3A4 inhibitors (clarithromycin, erythromycin, telithromycin, other
  • macrolide antibiotics, ketoconazole, itraconazole,
  • voriconazole,tolbutamide, ritonavir, atazanavir, indinavir, other HIV
  • protease inhibitors, verapamil, diltiazem, quinidine, digoxin, disulfiram)
  • or P-gp inhibitors (cyclosporine) at randomisation.
  • 8.Symptomatic peripheral neuropathy and pre-existing progressive
  • neuromuscular disease
  • 9.Inflammatory bowel disease (Crohn's or ulcerative colitis) or chronic
  • 10.Dementia, sufficient to impair independence in basic activities of
  • daily living.
  • 11.Active malignancy, known hepatitis B or C, or HIV infection.
  • 12.Impaired swallow preventing oral administration of Colchicine
  • 13.History of poor medication compliance.
  • 14.Unlikely to comply with study procedures due to severe or
  • fatalcomorbid illness or other factor (eg. inability to travel for follow up
  • visits), in opinion of randomising physician.
  • 15.Women of childbearing potential (WCBP), or pregnant or are
  • breastfeeding, are not eligible to participate in this study. (Clarification:
  • A woman of childbearing potential is a woman who:
  • - has not had surgery to remove the uterus and ovaries
  • - has had menstrual periods at any time in the preceding 24
  • consecutive months
  • - Menstrual periods interrupted due to cancer chemotherapy
  • treatment are considered WCBP as this may still allow conception.)
  • Pregnancy is considered highly unlikely during the trial because
  • women of childbearing potential are excluded. However, in the unlikely
  • event that a woman in the trial becomes pregnant, pregnancy
  • information will be collected.
  • 16.Patient concurrently participating in another clinical trial with an
  • investigational drug or device, or use of investigational drug within 30 or
  • 5 half-lives before the Screening visit (whichever is longer).
  • 17.Known allergy or sensitivity to colchicine.
  • 18.Requirement for colchicine therapy for treatment of acute gout,
  • gout prevention, or other rheumatological disorder
  • 19.Requirement for chronic daily immunosuppressants oral steroids, or
  • non-steroidal anti-inflammatory drugs (NSAIDs)

研究者

发起方
niversity College Dublin

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