Clinical Trials Directory

Trials / Completed

CompletedNCT01495481

Dexmedetomidine and Adenosine: Therapeutic Use for SVT

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
22 (actual)
Sponsor
University of Pittsburgh · Academic / Other
Sex
All
Age
5 Years – 30 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidineDexmedetomidine 2 mcg/kg, Intravenous push
DRUGAdenosineStepwise incremental approach of adenosine starting at 0.2 mg/kg (max 6 mg) followed by 0.3 mg/kg (max 12 mg) if initial dose was unsuccessful

Timeline

Start date
2012-01-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2011-12-20
Last updated
2017-03-28
Results posted
2017-03-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01495481. Inclusion in this directory is not an endorsement.