IRCT20220515054863N1招募中未知
Efficacy of compression stockings for treating recurrent vasovagal syncope: a triple-blind, multi-center, randomized controlled trial (COMFORTS-II)
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 268
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 65 years(—)
- 性别
- All
入选标准
- •Patients with 18 = age = 65 years
- •Vasovagal syncope as the cause of transient loss of conscious confirmed by Clinical diagnosis AndCalgary syncope system score (CSSS) =-2
- •=2 episodes of VVS during the last year
- •Capability of giving informed consent
排除标准
- •Orthostatic hypotension (decrease in BP =20/10 mmHg after 5-minute stand test)
- •Postural tachycardia (increase in heart rate =30 bpm after 5-minute stand test)
- •Carotid sinus hypersensitivity (ventricular pause >3 or decrease in BP > 50 mmHG after carotid sinus massage, performed in patients 40 years or older)
- •History of Seizure
- •Currently using medications for treatment of vasovagal syncope
- •Cardiac rhythm disorders including ventricular tachycardia, long QT syndrome, Brugada syndrome, arrhythmogenic right ventricular cardiomyopathy, complete heart block, or any conduction abnormality on ECG
- •Severe valvular heart disease
- •Hypertrophic cardiomyopathy
- •Cardiac systolic dysfunction (ejection fraction =40%)
- •Obstructive coronary artery disease
- •Cardiac implantable electronic devices
- •Prior recommendation of compression stocking by a health-care provider, or other indication for compression stocking use
- •Foot ulcers and diabetic foot
- •Chronic venous insufficiency
- •Renal failure stage =3 (eGFR <60 mL/min/1.73 m2)
- •Presence of a chronic severe illness
- •Pregnancy, or intention to become pregnant in the next year
- •Unwillingness to participate or to provide informed consent
研究者
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