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临床试验/CTRI/2021/01/030684
CTRI/2021/01/030684招募中未知

A RANDOMIZED TRIAL OF MODIFIED VALSALVA VERSUS STANDARD VALSALVA MANEUVER FOR CARDIOVERSION IN PATIENTS WITH SUPRAVENTRICULAR TACHYCARDIA IN EMERGENCY DEPARTMENT

Department of Emergency Medicine0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中

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

入选标准

  • 1.Patients/Legally Authorized Representative(LAR) providing Informed consent
  • 2. Diagnosis of supraventricular tachycardia (SVT; regular, narrow complex tachycardia with QRS duration <0.12 s on ECG with absent or overt p wave)

排除标准

  • I. Unable or unwilling to give informed consent
  • II. Unstable condition (systolic blood pressure (BP) <90 mm Hg or any indication for immediate drug or direct current cardioversion)
  • III. Atrial fibrillation/atrial flutter/sinus tachycardia/MAT on ECG
  • IV. Systemic hypoperfusion
  • i. Altered mentation
  • ii. Chest pain (due to coronary ischemia)
  • iii. Dyspnea (due to pulmonary edema)
  • V. Severe hypertension (systolic BP >220 mm Hg or diastolic BP >120 mm Hg)
  • VI. Any contraindication to or inability to performing a Valsalva maneuver
  • VII. Contraindication or inability to lay flat and have legs lifted (or any reason identified by the patient as to why this maneuver would cause discomfort or pain)
  • VIII. Pregnancy
  • IX. Myocardial Infarction( <3 months)
  • X. Known case of glaucoma or retinopathy
  • XI. Previous inclusion in the study

研究者

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