EUCTR2013-004919-43-IT进行中(未招募)不适用
Suspension of vasoactive drugs in reflex vasodepressive syncope: a randomized controlled trial
SOD Medicina e Cardiologia Geriatrica, Centro per lo Studio della Sincope - Università degli Studi di Firenze-AOUCareggi0 个研究点开始时间: 2014年4月28日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
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 on chronic therapy (> 1 year) with vasoactive drugs with recurrent reflex syncope (= 2 episodes / last year), for who it has been demonstrated positive tilt test or has been diagnosed with carotid sinus syndrome with predominantly vasodepressor component (form vasodepressor or mixed).
- •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 30
排除标准
- •1 - Patients with a diagnosis of symptomatic orthostatic hypotension, defined as a reduction in systolic blood pressure greater than 20 mmHg or diastolic blood pressure greater than 10 mmHg during the first 3 minutes after orthostatism.
- •2 - Patients with a diagnosis of syncope different from the vasodepressor reflex syncope
- •3 - Patients with reflex syncope with negativity of both carotid sinus massage and tilt test
- •4 - Patients with a clinical diagnosis of reflex syncope with cardioinihibiting component that requires pacemaker implantation
- •5 - Patients with poorly controlled hypertension (> 150/95)
- •6 - Patients with heart failure in the suspension / reduction therapy carries the risk of worsening the heart failure
- •7 - Patients with cardiac arrhythmias in which the suspension / reduction of antiarrhythmic therapy carries the risk of worsening arrhythmias
- •8 - Patients with prior TIA or stroke.
研究者
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