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临床试验/CTRI/2023/05/053279
CTRI/2023/05/053279招募中4 期

A prospective, post-market clinical data analysis in patients undergoing cardioversion ordefibrillation using Skanrays Defibrillators

Skanray Technologies Limited0 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
4 期
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
Observational

入排标准

入选标准

  • Data from the subject that meets the below-mentioned criteria shall be collected.
  • ? Patients with indications for defibrillation/cardioversion/pacing.
  • ? Male and female subjects who weigh above 10 kg.

排除标准

  • ? Unsafe conditions or surroundings for the use of Direct Current
  • ? Contraindications for defibrillation
  • A A responsive patient with spontaneous breathing and a palpable pulse.
  • B Asystole or pulseless electrical activity PEA
  • ? Contraindications for cardioversion - arrhythmias due to enhanced automaticity, such as
  • digitalis toxicity of digitalis-associated tachycardia, sinus tachycardia, multifocal atrial
  • tachycardia and junctional tachycardia. Catecholamine-induced arrhythmia having a
  • homogeneous depolarization state Eg CPVT, shall be excluded.
  • ? Contraindications for pacing - asymptomatic subjects with a reasonably stable rhythm.

研究者

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