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Rate Control in Atrial Fibrillation

Oral Propranolol, Diltiazem, Metoprolol and Verapamil in Atrial Fibrillation Rate Control in Patients With Stable Hemodynamic Status

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01655303
Enrollment
90
Registered
2012-08-01
Start date
2011-02-28
Completion date
2011-12-31
Last updated
2012-08-01

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

Conditions

Rapid Ventricular Response Atrial Fibrillation

Brief summary

Rate control in atrial fibrillation is a usual battle in emergency departments. Oral medications have a natural superiority to intravenous ones because they are easy-to-use and decrease the workload in busy emergency departments. This study wants to find an effective oral medication for rate control in rapid ventricular response atrial fibrillation. Propranolol and Metoprolol, Diltiazem and Verapamil are compared in patients with a stable hemodynamic status.

Interventions

DRUGPropranolol
DRUGMetoprolol
DRUGVerapamil
DRUGDiltiazem

Sponsors

Tehran University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age more than 18 years old * Stability in hemodynamic

Exclusion criteria

* Systolic blood pressure less than 90 mm Hg * Altered mental status attributable to rapid ventricular response atrial fibrillation * Acute pulmonary edema attributable to rapid ventricular response atrial fibrillation * Chest pain attributable to rapid ventricular response atrial fibrillation * Allergy to Propranolol or Metoprolol or Verapamil or Diltiazem * History of asthma

Design outcomes

Primary

MeasureTime frameDescription
Rate less than 100 per minuteIn 1 hourVentricular rate less than 100 per minute after 1 hour of per oral medication administration

Secondary

MeasureTime frameDescription
Drugs adverse effects2 hoursDrugs adverse effects seen in patients in 2 hours after per oral medication administration
Unstability in hemodynamic2 hoursHemodynamic instability (systolic blood pressure less than 90 mmHg, loss of consciousness, pulmonary edema, chest pain)

Countries

Iran

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026