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The effects of Amiodarone for control of heart rate in patients with rapid ventricular response atrial fibrillation

Comparison of Amiodarone and Digoxin in controlling rapid ventricular response atrial fibrillation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201206047449N2
Enrollment
108
Registered
2012-11-02
Start date
2012-03-20
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial fibrillation. Atrial fibrillation and flutter

Interventions

Intervention 1: for internention: Intravenous Amiodarone 150 mg over 10 minutes followed by a 50 mg per hour slow infusion for 3 hours then 25 mg per hour for 8 hours. Intervention 2: For control: Di
Treatment - Drugs
for internention: Intravenous Amiodarone 150 mg over 10 minutes followed by a 50 mg per hour slow infusion for 3 hours then 25 mg per hour for 8 hours.
For control: Digoxin is given in an initial slow intravenous dose of 0.5 mg then if needed 0.25 mg in hours 2 and 4 of intervention.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients with over 110 beats per minute Atrial Fibrillation who are referred to emergency room Exclusion criteria: patients with unstable vital signs who are needed electrical cardioversion; or due to underline diseases such as sepsis, anemia, bleeding, hypovolemia who are needed treatment under 18 or over 80 years; who haven't congestive heart failure; who have received antiarrhythmic agents last 12 hours; who couldn't monitoring 12 hours during the study who are not willing to participate in this study; presence of hepatic or renal dysfunction; atrial fibrillation diagnosis isn't definite in ECG;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Heart rate. Timepoint: Before the intervention,and during 12 hours of the intervention and one week after intervention. Method of measurement: Heart rate based on ECG and cardiac monitoring.

Secondary

MeasureTime frame
Time to response. Timepoint: During 12 hours of intervention. Method of measurement: Heart rate based on ECG and cardiac monitoring.;Decrease in blood pressure more than 20 mmHg. Timepoint: During 12 hours of intervention. Method of measurement: Standard sphygmomanometer 2 times with 2 persons.;Decrease in heart rate less than 60 beats per minute. Timepoint: Every 1 hour during 12 hours of intervention. Method of measurement: Heart rate based on ECG and cardiac monitoring.;Occurrence of other arrhythmias. Timepoint: During 12 hours of intervention. Method of measurement: Based on ECG and cardiac monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Majid Shojaee

Shahid Beheshti Medical University

m.shojaee@sbmu.ac.ir+98 21 7343 2380

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026