Clinical Trials Directory

Trials / Completed

CompletedNCT00268554

Enhancement of Postocclusive Reactive Hyperaemia by Dipyridamole

Enhancement of Postocclusive Reactive Hyperaemia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
12 (estimated)
Sponsor
Radboud University Medical Center · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine whether dipyridamole enhances postocclusive reactive hyperaemia by increasing extracellular adenosine concentrations during ischemia and reperfusion. Furthermore we hypothesize that dipyridamole augments postocclusive reactive hyperaemia by increasing adenosine receptor stimulation.

Conditions

Interventions

TypeNameDescription
DRUGdipyridamole
DRUGcaffeine

Timeline

Start date
2005-12-01
Completion
2006-07-01
First posted
2005-12-22
Last updated
2008-03-28

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00268554. Inclusion in this directory is not an endorsement.