Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The 'Electrical-first' protocol is a sequential treatment strategy for acute atrial fibrillation developed and studied by the University of British Columbia (specifically in the RAFF trial). This intervention arm prioritizes synchronized electrical cardioversion over pharmacological rhythm control. The procedure begins with patient sedation, typically using propofol (0.5 - 1.0 mg/kg), followed by up to three synchronized electrical shocks (100 J, 200 J, 200 J). If the patient remains in atrial fibrillation after the third shock, the protocol proceeds to chemical cardioversion using intravenous procainamide (17 mg/kg administered over 30 minutes). This approach is designed to optimize the speed of rhythm conversion and reduce emergency department length-of-stay compared to strategies that lead with antiarrhythmic medications.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Electrical-first cardioversion protocol.