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Dexmedetomidine and Adenosine: Therapeutic Use for SVT

Not Applicable
Completed
Conditions
Supraventricular Tachycardia
Interventions
Registration Number
NCT01495481
Lead Sponsor
University of Pittsburgh
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
22
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Adenosine and DexmedetomidineDexmedetomidinePatients will receive adenosine and then dexmedetomidine for the termination of SVT
Adenosine and DexmedetomidineAdenosinePatients will receive adenosine and then dexmedetomidine for the termination of SVT
Primary Outcome Measures
NameTimeMethod
Termination of SVTWithin 3 minutes

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

Secondary Outcome Measures
NameTimeMethod
Number of Participants With Sinus Pause >2.5 Sec After Termination of SVT1 minute

Evaluation of the number of participants with sinus pause \> 2.5 sec, after dexmedetomidine vs. adenosine induced SVT termination

Number of Participants With Tachyarrhythmias After Medication Administration10 minutes

Number of participants with tachyarrhythmias, including Ventricular (Ventricular Tachycardia \& Fibrillation)and supraventricular (Atrial Flutter \& Fibrillation) after dexmedetomidine vs. adenosine administration

Number of Participants With Hypotension by Non-invasive Cuff in First 10 Minutes After Medication Administration10 minutes

Blood pressure changes after dexmedetomidine vs. adenosine. Blood pressure measured by non-invasive cuff prior to medication administration, and then at 1 min, 3 min, 5 min after medication administration. Number of participants with a significant drop in blood pressure (mmHg) compared to baseline would be counted for hypotension.

Trial Locations

Locations (1)

Childrens Hospital of Pittsburgh of UPMC

🇺🇸

Pittsburgh, Pennsylvania, United States

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