Trials / Completed
CompletedNCT01809743
Regadenoson and Adenosine
Comparison of Regadenoson (Rapiscan) and Central Intravenous Adenosine for Measurement of Fractional Flow Reserve
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Lokien van Nunen · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The aim of the study is to test the accuracy of Regadenoson to induce maximal and steady state hyperemia as compared to central venous infusion of adenosine for assessing fractional flow reserve. (adenosine is considered to be the gold standard)and to investigate the time intervals of maximum hyperemia induced by centrally and peripherally administered Regadenoson.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Regadenoson central -central | To test the accuracy of Regadenoson to induce maximal and steady state hyperemia as compared to central venous infusion of adenosine for assessing fractional flow reserve. (adenosine is considered to be the golden standard). |
| DRUG | Regadenoson peripheral - peripheral | To test the accuracy of Regadenoson to induce maximal and steady state hyperemia as compared to central venous infusion of adenosine for assessing fractional flow reserve. (adenosine is considered to be the golden standard). |
| DRUG | Regadenoson central - peripheral | To test the accuracy of Regadenoson to induce maximal and steady state hyperemia as compared to central venous infusion of adenosine for assessing fractional flow reserve. (adenosine is considered to be the golden standard). |
| DRUG | Regadenoson peripheral - central | To test the accuracy of Regadenoson to induce maximal and steady state hyperemia as compared to central venous infusion of adenosine for assessing fractional flow reserve. (adenosine is considered to be the golden standard). |
| DRUG | Adenosine | Fractional flow reserve is measured by inducing hyperaemia using central adenosine infusion. |
Timeline
- Start date
- 2013-01-01
- Primary completion
- 2013-10-01
- Completion
- 2013-10-01
- First posted
- 2013-03-13
- Last updated
- 2013-11-13
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT01809743. Inclusion in this directory is not an endorsement.