Skip to main content
Clinical Trials/NCT01495481
NCT01495481
Completed
Not Applicable

Dexmedetomidine Versus Adenosine: Electrophysiologic Effects and Therapeutic Use for Terminating Supraventricular Tachycardia

University of Pittsburgh1 site in 1 country22 target enrollmentJanuary 2012

Overview

Phase
Not Applicable
Intervention
Dexmedetomidine
Conditions
Supraventricular Tachycardia
Sponsor
University of Pittsburgh
Enrollment
22
Locations
1
Primary Endpoint
Termination of SVT
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the efficacy and safety of dexmedetomidine in the acute termination of Supraventricular Tachycardia (SVT).

Detailed Description

In 2006 the investigator found that dexmedetomidine, an alpha-2 adrenergic agonist with primarily sedative properties, possesses additional anti-arrhythmic properties. So far the investigator has found that dexmedetomidine has the ability to prevent or terminate arrhythmias like atrial ectopic tachycardia (85% success) and junctional ectopic tachycardia (75% success). The most dramatic effect however was observed in the acute termination of reentrant SVT with a success rate of \> 96%. More importantly we found that dexmedetomidine terminates SVT without causing any sinus pause or asystole (frequently seen with adenosine) and thus avoiding the feeling of "impending doom". In this study adenosine is being compared head to head with dexmedetomidine in a cross over study, for both safety and efficacy when given for the termination of SVT in the electrophysiology (EP) lab. Additional EP parameters will be measured to elucidate the exact site of dexmedetomidine's mechanism of action.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
July 2014
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Gaurav Arora

Assistant Professor

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • Patients between the age of 5 - 30 years old, who are scheduled for cardiac electrophysiology study for evaluation of reentrant SVT

Exclusion Criteria

  • Severe Heart Failure
  • Presence of of any other antiarrhythmic medication within 24 hours of enrollment
  • Third degree heart block
  • Sick Sinus Syndrome

Arms & Interventions

Adenosine and Dexmedetomidine

Patients will receive adenosine and then dexmedetomidine for the termination of SVT

Intervention: Dexmedetomidine

Adenosine and Dexmedetomidine

Patients will receive adenosine and then dexmedetomidine for the termination of SVT

Intervention: Adenosine

Outcomes

Primary Outcomes

Termination of SVT

Time Frame: Within 3 minutes

Number of participants with SVT Termination within 3 minutes of medication administration

Secondary Outcomes

  • Number of Participants With Sinus Pause >2.5 Sec After Termination of SVT(1 minute)
  • Number of Participants With Tachyarrhythmias After Medication Administration(10 minutes)
  • Number of Participants With Hypotension by Non-invasive Cuff in First 10 Minutes After Medication Administration(10 minutes)

Study Sites (1)

Loading locations...

Similar Trials