EUCTR2016-001219-18-DK进行中(未招募)1 期
Effect of glucagon-like peptide 1 (GLP-1) based diabetes medication on blood flow velocity in ischemic stroke patients - GLP-1 and apoplexia
Herlev Gentofte Hospital0 个研究点目标入组 30 人开始时间: 2016年3月22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
- 30
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
- •Patients = 18 years with new-onset symptoms of stroke
- •Must be able to receive GLP-1 RA / placebo medication within 21 days after the onset of symptoms
- •Radiological verified diagnosis of stroke
- •NIHSS between 1-20 at the onset of symptoms
- •mRS = 2 prior to onset of symptoms
- •Has given 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 10
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 20
排除标准
- •Intracerebral haemorrhage
- •Subdural / epidural hemorrhage
- •subarachnoid haemorrhage
- •previously major structural damage to the brain (eg. sequelae after large stroke or brain surgery)
- •Type 1 diabetes
- •Type 2 diabetes
- •Known atrial fibrillation
- •> 50% stenosis of halskar
- •Known allergy to GLP-1 RA preparations
- •Hepatic impairment (ALT> 3 x upper normal limit)
- •Renal impairment (eGFR <30 ml / min)
- •Inflammatory bowel disease
- •Previous pancreatitis
- •Heart failure (NYHA class 3-4)
- •Pregnancy or lactation
- •Patient is not expected to co-operate to the investigations
- •Visualization of the middle cerebral artery bilaterally by transcranial doppler not possible
研究者
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