- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00457405
Does a Seven Day Treatment With Dipyridamole Induce Protection Against Ischemia-Reperfusion Injury?
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Rationale:
Dipyridamole increases the endogenous adenosine level by inhibition of the nucleoside transporter (ENT-1). Activation of the adenosine receptor protects against ischemia-reperfusion injury (pharmacologic preconditioning).
The purpose of this project is to explore whether a seven day treatment with dipyridamole can reduce ischemia-reperfusion injury in the forearm, in a randomized double blind placebo controlled trial.
Study design:
Randomized double-blind placebo-controlled trial with a cross-over design.
Study population:
Healthy male volunteers, aged 18-50 yr
Intervention:
10 Volunteers will be randomised to receive in a cross-over design either a 7 day treatment with dipyridamole (Persantin retard; 200 mg twice daily) or placebo followed by 10 minutes of ischemic isometric muscle contraction of the non-dominant forearm and upon reperfusion infusion of radiolabeled Annexin A5 (Annexin scintigraphy).
Main study parameters/endpoints:
Percentage difference in radioactivity (counts/pixel) between experimental and control thenar muscle at 60 and 240 minutes after reperfusion.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness:
This study will be executed at the Clinical Research Centre Nijmegen under close medical supervision. Treatment with dipyridamole is not expected to harm the volunteers. During the first days of treatment with dipyridamole, a headache may occur. Ischemic hand gripping will temporarily result in pain in the forearm. This is completely reversible upon reperfusion. Administration of radiolabeled Annexin A5 results in an effective dose of less than 5 mSv, well within the range of accepted exposure to radioactivity for human research. Participation in this research does not interfere with possible diagnostic or therapeutic procedures with X-rays of radioactivity in the future.
Occurrence of an allergic reaction is theoretically possible upon administration of Annexin A5, however there have been no allergic reactions reported in all volunteers exposed to Annexin A5.
The volunteers will not benefit directly from participating in this study.
Study Type
Enrollment (Actual)
Phase
- Phase 4
Contacts and Locations
Study Locations
-
-
-
Nijmegen, Netherlands, 6500HB
- Radboud University Nijmegen Medical Centre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Male
- age between 18-50yr.
Exclusion Criteria:
- cardiovascular disease
- hypertension (systole > 140 mmHg, diastole > 90 mmHg)
- hypercholesterolemia (fasting total cholesterol > 5.5 mmol/l or not fasting total cholesterol > 6.5mmol/L)
- diabetes mellitus (fasting glucose > 7.0 mmol/L or random glucose > 11.0 mmol/L)
- asthma (recurrent episodes of dyspnea and wheezing, or usage of prescribed inhalation medication: i.e. corticosteroids or B2-agonists)
- participation in any clinical trial during the last 60 days prior to this study.
- administration of any radioactivity for research purposes during the last 5 years prior to this study.
- concomitant medication
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: 1
first 7 day treatment with dipyridamol and at least two weeks later 7 day treatment with placebo
|
dipyridamole 200mg twice daily
Other Names:
|
Active Comparator: 2
first 7 day treatment with placebo and at least two weeks later 7 day treatment with atorvastatin
|
dipyridamole 200mg twice daily
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Percentage difference in radioactivity (counts/pixel) between experimental and control thenar muscle at 60 and 240 minutes after reperfusion.
Time Frame: 60 and 240 minutes after reperfusion
|
60 and 240 minutes after reperfusion
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Plasma dipyridamole concentration
Time Frame: in the morning of day seven of treatment
|
in the morning of day seven of treatment
|
Workload (duration of exercise and developed force)
Time Frame: during 10 minutes ischemic exercise
|
during 10 minutes ischemic exercise
|
Heart rate (preceded by a 7day treatment of dipyridamol or placebo)
Time Frame: during 30 minutes at day seven of treatment with dipyridamol and placebo
|
during 30 minutes at day seven of treatment with dipyridamol and placebo
|
Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Cardiovascular Diseases
- Vascular Diseases
- Arteriosclerosis
- Arterial Occlusive Diseases
- Postoperative Complications
- Ischemia
- Wounds and Injuries
- Reperfusion Injury
- Atherosclerosis
- Molecular Mechanisms of Pharmacological Action
- Vasodilator Agents
- Enzyme Inhibitors
- Platelet Aggregation Inhibitors
- Phosphodiesterase Inhibitors
- Dipyridamole
Other Study ID Numbers
- dipy003
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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