Clinical Trials Directory

Trials / Completed

CompletedNCT01070420

Comparison of Hyperemic Efficacy Between Central and Peripheral Adenosine Infusion for Fractional Flow Reserve (FFR) Measurement

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
66 (estimated)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety and effectiveness of the peripheral IV continuous infusion without the insertion of central venous vascular access method in the achievement of steady-state maximal coronary hyperemia compared with the central IV continuous infusion method.

Conditions

Interventions

TypeNameDescription
OTHERFFR via central venous linePatients with intermediate coronary artery stenosis were consecutively enrolled. FFR was measured by a standard intravenous (IV) adenosine infusion (140 μg•min-1•kg-1) via Rt central femoral vein.
OTHERFFR via peripheral venous linePatients with intermediate coronary artery stenosis were consecutively enrolled. FFR was measured by a standard intravenous (IV) adenosine infusion (140 μg•min-1•kg-1) via continuous peripheral vein.

Timeline

Start date
2009-12-01
Primary completion
2011-04-01
Completion
2011-05-01
First posted
2010-02-18
Last updated
2011-07-18

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01070420. Inclusion in this directory is not an endorsement.