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临床试验/IRCT20220515054863N1
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)

Tehran University of Medical Sciences0 个研究点目标入组 268 人开始时间: 待定最近更新:
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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