Oral Verapamil in Acute Paroxysmal Supra Ventricular Tachycardia(PSVT) Recurrence Control
This study has been completed.
Sponsor:
Tehran University of Medical Sciences
Information provided by (Responsible Party):
Tehran University of Medical Sciences
ClinicalTrials.gov Identifier:
NCT01655316
First received: July 30, 2012
Last updated: November 12, 2012
Last verified: November 2012
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Purpose
PSVT is a common rhythm disorder in emergency department which can be recurrent in some cases.
Intravenous Adenosine is the drug of choice in PSVT control in acute settings but is a very short acting agent.
Providing a complementary medication to decrease the rate of recurrence of PSVT after its initial control will be promising.
This study evaluates the role of the oral Verapamil in recurrence control of PSVT in emergency situations.
| Condition | Intervention | Phase |
|---|---|---|
|
Paroxysmal Supraventricular Tachycardia |
Drug: Verapamil |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Single Blind (Subject) Primary Purpose: Treatment |
Resource links provided by NLM:
Drug Information available for:
Verapamil hydrochloride
Diltiazem hydrochloride
Diltiazem
Diltiazem malate
U.S. FDA Resources
Further study details as provided by Tehran University of Medical Sciences:
Primary Outcome Measures:
- Recurrence Control [ Time Frame: 2 hours ] [ Designated as safety issue: No ]
| Enrollment: | 90 |
| Study Start Date: | October 2010 |
| Study Completion Date: | August 2011 |
| Primary Completion Date: | August 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Verapamil
40 mg Verapamil Per Oral
|
Drug: Verapamil |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Age>18 years old
- PSVT on emergency department presentation
Exclusion Criteria:
- Instability in hemodynamic status
- Allergy to Verapamil
Contacts and Locations
No Contacts or Locations Provided
More Information
No publications provided
| Responsible Party: | Tehran University of Medical Sciences |
| ClinicalTrials.gov Identifier: | NCT01655316 History of Changes |
| Other Study ID Numbers: | 16062 |
| Study First Received: | July 30, 2012 |
| Last Updated: | November 12, 2012 |
| Health Authority: | Iran: Ministry of Health |
Additional relevant MeSH terms:
|
Tachycardia, Supraventricular Tachycardia Tachycardia, Ventricular Arrhythmias, Cardiac Heart Diseases Cardiovascular Diseases Pathologic Processes Verapamil Diltiazem |
Vasodilator Agents Cardiovascular Agents Therapeutic Uses Pharmacologic Actions Anti-Arrhythmia Agents Calcium Channel Blockers Membrane Transport Modulators Molecular Mechanisms of Pharmacological Action Antihypertensive Agents |
ClinicalTrials.gov processed this record on June 18, 2013