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Condition: Electric Countershock Synced from ClinicalTrials.gov · July 29, 2026

Recruiting studies: Electric Countershock

Studies currently listed as recruiting on the public registry for this search term. Each page explains the study in plain language, with locations and the study team's contact details. Clinicians: generate a printable list for your patient →

Left Atrial Imaging Prior to Cardioversion: Leveraging Computed Tomography to Rule Out Thrombus in The Emergency Departm
NA · 3 location(s) · Ottawa Heart Institute Research Corporation · NCT07002450
The SAFE Prospective Registry
NA · 1 location(s) · University Hospital Ostrava · NCT05794464
Left Atrial Volume Changes Who Underwent Cardioversion and Recurrence of AF After RF Ablation in Persistent AF (SAFE-AF)
Phase N/A · 1 location(s) · The Second Affiliated Hospital of Chongqing Medical Universi · NCT06523738
Shock Energy for Electrical Cardioversion of Persistent Atrial Fibrillation
NA · 1 location(s) · Wellington Hospital · NCT05903170
Anteroposterior Versus Anterolateral Electrode Position for Electrical Cardioversion of Atrial Fibrillation
NA · 4 location(s) · McMaster University · NCT05511389
RECURrence of Atrial Fibrillation After Cardioversion of Patients Randomized to Dapagliflozin or Usual Care
Phase 3 · 7 location(s) · Region Stockholm · NCT07187570
Initial Double Sequential External Defibrillation in Out of Hospital Cardiac Arrest
NA · 1 location(s) · St. Olavs Hospital · NCT06672159
Electrophysiological Registry Duesseldorf
Phase N/A · 1 location(s) · Heinrich-Heine University, Duesseldorf · NCT07196176
QOL Improvement After Cardioversion of Persistent AF (QOL-CAFRCT)
NA · 2 location(s) · Ottawa Heart Institute Research Corporation · NCT05136131
Parasternal Extravascular ICD System Pivotal Clinical Investigation (ALARION EV) Study
NA · 35 location(s) · AtaCor Medical, Inc. · NCT07324031
The DefiPace Study
Phase N/A · 10 location(s) · Institut für Pharmakologie und Präventive Medizin · NCT04804748
Multimodal Cardiac Imaging Registry in Patients with Atrial Fibrillation
Phase N/A · 7 location(s) · University in Zielona Góra · NCT06584266
BIS-Guided Sedation Versus Standard Clinical Sedation During Elective Electrical Cardioversion for Atrial Fibrillation
NA · 1 location(s) · Istanbul University - Cerrahpasa · NCT07569016
Stepwise Strategy for Treatment of Atrialfibrillation Substrate Study
Phase N/A · 1 location(s) · Yuehui Yin · NCT07129564
MAX - SHOCK Clinical Trial
NA · 1 location(s) · Ottawa Heart Institute Research Corporation · NCT06556667
Evaluation of Two Different Regimens of the Antiarrhythmic Drug Amiodarone to Maintain Normal Sinus Rhythm After Electri
Phase 4 · 1 location(s) · Fundació Institut de Recerca de l'Hospital de la Santa Creu · NCT07273994
Flecainide Versus Amiodarone in the Cardioversion of Paroxysmal Atrial Fibrillation at the Emergency Department, in Pati
Phase 3 · 3 location(s) · Hippocration General Hospital · NCT05549752
Investigation of Cardioversion Versus Therapeutic Ablation for Persistent AF (ORBICA-AF)
NA · 1 location(s) · Barts & The London NHS Trust · NCT06096246
Strategies for Defibrillation During Out-of-Hospital Cardiac Arrest
NA · 6 location(s) · Lars Wiuff Andersen · NCT06781892
Repeat Ablation of Persistent Atrial Fibrillation, Including Mitral Isthmus Catheter Ablation, With the FARAPULSE Pulsed
NA · 41 location(s) · Boston Scientific Corporation · NCT06735534
Electrical Cardioversion As a Predictor in Postoperative Preservation of Sinus Rhythm
NA · 1 location(s) · Saint Petersburg State University, Russia · NCT06654401
Pulmonary Vein Isolation Alone or in Combination With Substrate Modulation After Electric Cardioversion Failure
NA · 13 location(s) · Elsan · NCT05264831
Early Double Sequential Defibrillation in Out of Hospital Cardiac Arrest
Phase 2/Phase 3 · 14 location(s) · Gabriel Riva · NCT07174986
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.