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
| Type | Name | Description |
|---|---|---|
| OTHER | Maximal Hyperemia with Adenosine Followed by Nicorandil | Firstly 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). |
| OTHER | Maximal Hyperemia with Nicorandil Followed by Adenosine | Firstly 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.