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Efficacy and safety of Iranian Avecinna co. defibrillator

Not Applicable
Recruiting
Conditions
Atrial fibrillation, atrial flutter.
Atrial fibrillation and flutter
Registration Number
IRCT20230809059099N2
Lead Sponsor
Avecinna co
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
105
Inclusion Criteria

Age >18 years old
Atrial fibrillation or flutter
indication for cardioversion
Atrial fibrillation or flutter will be confirmed by an electrophysiologist using 12 lead standard ECG. Cardioversion will be conducted at the discretion of the electrophysiologist.
All patients are required to receive at least 4 weeks of antio coagulation or left atrial thrombus is ruled out by trans esophageal echocardiography

Exclusion Criteria

Requiring emergeny cardioversion
Hemodynamic instability
Chest pain or suspicion of acute coronary syndrome
Hypokalemia
Digoxin toxicity
Pregnancy or breastfeeding
No informed consent

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Rate of sinus rhythm conversion. Timepoint: After cardioversion. Method of measurement: ECG.
Secondary Outcome Measures
NameTimeMethod
umber of times shock is required in experimental and standard device. Timepoint: After start of the cardioversion process. Method of measurement: Number.;Safety: any inflammation, burn, pain, or electrocution in experimental device compared to standard device. comparison of ventricular arrhythmias, bradycardia, or asystole.comparison of any other adverse effects. Timepoint: Immeadiately after shock. Method of measurement: Observation by the cardiologist.
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