Clinical Trials Directory

Trials / Completed

CompletedNCT00430170

Does Caffeine Reduce Dipyridamole-Induced Protection Against Ischemia-Reperfusion Injury?

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Radboud University Medical Center · Academic / Other
Sex
Male
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this project is to explore the interaction between caffeine and dipyridamole on ischemia-reperfusion injury in the forearm.

Detailed description

Dipyridamole has been proven to reduce targeting of Annexin A5 in responses to ischemic exercise, indicating protection against ischemia-reperfusion injury in humans (pharmacological preconditioning). Dipyridamole increases the endogenous adenosine level by inhibition of the nucleoside transporter (ENT-1). Activation of the adenosine receptor protects against ischemia-reperfusion injury. We hypothesize that endogenous adenosine mediates the protective effect of dipyridamole against ischemia-reperfusion injury. Therefore the adenosine receptor antagonist caffeine will reduce the benefit of dipyridamole on forearm ischemia-reperfusion injury.

Conditions

Interventions

TypeNameDescription
DRUGDipyridamoleDipyridamole 2x200mg 7day per os
DRUGcaffeinecaffeine 4mg/kg iv

Timeline

Start date
2007-01-01
Primary completion
2007-03-01
Completion
2007-04-01
First posted
2007-02-01
Last updated
2008-07-29

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00430170. Inclusion in this directory is not an endorsement.