Rate Control in Atrial Fibrillation
Information source: Tehran University of Medical Sciences
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Rapid Ventricular Response Atrial Fibrillation
Intervention: Propranolol (Drug); Metoprolol (Drug); Verapamil (Drug); Diltiazem (Drug)
Phase: Phase 4
Status: Completed
Sponsored by: Tehran University of Medical Sciences
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.
Clinical Details
Official title: Oral Propranolol, Diltiazem, Metoprolol and Verapamil in Atrial Fibrillation Rate Control in Patients With Stable Hemodynamic Status
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment
Primary outcome: Rate less than 100 per minute
Secondary outcome: Drugs adverse effectsUnstability in hemodynamic
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
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
Locations and Contacts
Rasoul-e-Akram Hospital, Tehran 14436151, Iran, Islamic Republic of
Additional Information
Starting date: February 2011
Last updated: July 30, 2012
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