Clin2
NCT05511389Possibly a fitRecruiting

Testing better electrode placement for heart rhythm shock

Atrial FibrillationAtrial Flutter

Part of Heart & circulation clinical trials.

This study tests whether two different positions of the electrodes (pads) used for an electrical shock work equally well for people with atrial fibrillation or flutter. It may help improve how safely and effectively the shock restores a normal rhythm.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
1,750 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are an adult and can give consent for the study
  • You are scheduled for a planned (non-emergency) electrical shock to treat atrial fibrillation or atrial flutter
  • Your blood-thinning medicine plan is enough for the planned cardioversion, per Canadian guidelines
  • You must have had a transesophageal echocardiogram (a probe ultrasound through the throat) to check for a blood clot in the heart
  • Your skin and body structure allow electrode placement in either the front-left (anterolateral) or front-center (anteroposterior) areas, with no major wounds or skin problems there

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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