Heart Rate Response to Regadenoson and Sudden Cardiac Death

NACompletedINTERVENTIONAL
Enrollment

90

Participants

Timeline

Start Date

February 28, 2013

Primary Completion Date

April 30, 2020

Study Completion Date

July 31, 2022

Conditions
Left Ventricular Systolic DysfunctionSudden Cardiac Death
Interventions
DRUG

regadenoson

Prior to the implantation of a clinically indicated ICD, the heart rate response to regadenoson will be assessed. Regadenoson will be administered intravenously as a fixed intravenous bolus dose of 400 μg followed by a 5 mL saline flush. Medications (including beta-blockers) will be withheld on the morning of the test. The heart rate and blood pressure will be measured at baseline and every minute after regadenoson bolus for at least 5 minutes and until the heart rate and blood pressure are clearly returning towards baseline.

Trial Locations (1)

35294

UAB, Birmingham

All Listed Sponsors
collaborator

Astellas Scientific & Medical Affairs, Inc.

INDUSTRY

lead

University of Alabama at Birmingham

OTHER

NCT01842035 - Heart Rate Response to Regadenoson and Sudden Cardiac Death | Biotech Hunter | Biotech Hunter