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
| Type | Name | Description |
|---|---|---|
| OTHER | FFR via central venous line | Patients 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. |
| OTHER | FFR via peripheral venous line | Patients 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.