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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00268554
Other study ID # PORH-dipy
Secondary ID
Status Completed
Phase N/A
First received December 21, 2005
Last updated March 27, 2008
Start date December 2005
Est. completion date July 2006

Study information

Verified date March 2008
Source Radboud University
Contact n/a
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date July 2006
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- healthy volunteers between 18 and 50 years

Exclusion Criteria:

- none specified

Study Design

Allocation: Non-Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Drug:
dipyridamole

caffeine


Locations

Country Name City State
Netherlands Radboud university Nijmegen Medical Centre Nijmegen Gelderland

Sponsors (1)

Lead Sponsor Collaborator
Radboud University

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary forearm blood flow
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