Clinical Trials Directory

Trials / Unknown

UnknownNCT01331902

Comparison of Hyperemic Efficacy Between Nicorandil and Adenosine for Fractional Flow Reserve (FFR) Measurement

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
200 (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 efficacy of nicorandil in the achievement of maximal coronary hyperemia compared with adenosine.

Conditions

Interventions

TypeNameDescription
OTHERMaximal Hyperemia with Adenosine Followed by NicorandilFirstly FFR was measured with intravenous adenosine infusion (140 μg•min-1•kg-1) via femoral vein or antecubital vein. Secondly with intracoronary adenosine bolus injection (80μg, 40μg to LCA and RCA, respectively). Lastly with intracoronary nicorandil bolus injection (1mg followed by 2mg).
OTHERMaximal Hyperemia with Nicorandil Followed by AdenosineFirstly FFR was measured with intracoronary nicorandil bolus injection (1mg followed by 2mg). Secondly with intravenous adenosine infusion (140 μg•min-1•kg-1) via femoral vein or antecubital vein. Lastly with intracoronary adenosine bolus injection (80μg, 40μg to LCA and RCA, respectively).

Timeline

Start date
2011-03-01
Primary completion
2011-09-01
Completion
2011-09-01
First posted
2011-04-08
Last updated
2011-04-08

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01331902. Inclusion in this directory is not an endorsement.