Clinical Trials Directory

Trials / Completed

CompletedNCT04249258

Dobutamine on the Cardiac Conduction System

The Effects of Dobutamine on the Cardiac Conduction System: Site-Specific Dose

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
37 (actual)
Sponsor
Northwell Health · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

Our hypothesis is that Dobutamine will act in a similar fashion to Isoproterenol with respect to cardiac conduction. Our goal is to study the effects of Dobutamine on cardiac conduction and refractoriness during an Electrophysiology study (EPS). At the end of most EPS Isoproterenol is commonly administered in an effort to change the conduction properties of the heart. In our practice we have been using Dobutamine for this purpose for many years. Dobutamine has never been rigorously studied for this indication however. We designed this study to systematically study the effect of various doses of Dobutamine on the parameters of cardiac conduction and refractoriness that are commonly measured during an EPS. We are specifically looking to compare the effect that Dobutamine has on the sinus node with the effect it has on the atrioventricular node. Patients undergoing an EPS at Long Island Jewish Hospital will be recruited and consented. Measurements of various conduction parameters will be taken at baseline as is standard protocol for an EPS. Dobutamine will then be administered at doses of 5mcg/kg/min, 10mcg/kg/min, 15mcg/kg/min and 20mcg/kg/min. At each of these dosages the same conduction parameters will be measured. A comparison will then be made between the conduction parameters at baseline and when the Dobutamine is administered.

Conditions

Interventions

TypeNameDescription
DRUGDobutamineDobutamine will then be administered at doses of 5mcg/kg/min, 10mcg/kg/min, 15mcg/kg/min and 20mcg/kg/min.

Timeline

Start date
2020-01-14
Primary completion
2021-11-20
Completion
2021-11-20
First posted
2020-01-30
Last updated
2022-01-26

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04249258. Inclusion in this directory is not an endorsement.