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| Sponsor: | University of Wisconsin, Madison |
|---|---|
| Collaborator: |
Astellas Pharma US, Inc. |
| Information provided by: | University of Wisconsin, Madison |
| ClinicalTrials.gov Identifier: | NCT00205166 |
Purpose
We are studying the affect of caffeine on the sensitivity of detecting coronary artery disease (blockages in the blood flow to the heart) with adenosine tracer scans. Adenosine is a drug used routinely in patients to relax heart blood vessels in order to assess for the presence of coronary artery disease. Often, if patients have had caffeine, the adenosine scan is not used because of the belief that caffeine may reduce the ability to detect coronary artery disease. We would like to test whether caffeine affects our ability to detect coronary artery disease with adenosine tracer scanning. We will perform an imaging study of the heart with adenosine after you have received caffeine.
| Condition | Intervention |
|---|---|
|
Coronary Artery Disease |
Procedure: Cardiac SPECT imaging Rest and Stress Drug: Caffeine |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Diagnostic |
| Official Title: | Does Caffeine Affect the Sensitivity of Adenosine Perfusion Scans? |
| Estimated Enrollment: | 50 |
| Study Start Date: | June 1999 |
| Estimated Study Completion Date: | December 2008 |
| Estimated Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: 1
Caffeine 400 mg PO 1 hour before adenosine infusion
|
Procedure: Cardiac SPECT imaging Rest and Stress
adenosine perfusion scintigraphy
Drug: Caffeine
Caffeine 400 mg po
|
|
Active Comparator: 2
Caffeine 200 mg po one hour before adenosine infusion
|
Procedure: Cardiac SPECT imaging Rest and Stress
adenosine perfusion scintigraphy
Drug: Caffeine
Caffeine 200 mg po
|
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, Wisconsin | |
| University of Wisconsin | |
| Madison, Wisconsin, United States, 53792 | |
| Principal Investigator: | Charles K Stone, MD | Univeristy of Wisconsin |
More Information
| Responsible Party: | Charles K. Stone, MD, University of Wisconsin |
| ClinicalTrials.gov Identifier: | NCT00205166 History of Changes |
| Other Study ID Numbers: | 1999-109 |
| Study First Received: | September 12, 2005 |
| Last Updated: | May 16, 2008 |
| Health Authority: | United States: Institutional Review Board |
|
adenosine tracer scans coronary artery disease caffeine |
|
Coronary Artery Disease Myocardial Ischemia Coronary Disease Heart Diseases Cardiovascular Diseases Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases Adenosine Caffeine Analgesics Sensory System Agents Peripheral Nervous System Agents Physiological Effects of Drugs |
Pharmacologic Actions Central Nervous System Agents Therapeutic Uses Anti-Arrhythmia Agents Cardiovascular Agents Vasodilator Agents Central Nervous System Stimulants Phosphodiesterase Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Purinergic P1 Receptor Antagonists Purinergic Antagonists Purinergic Agents Neurotransmitter Agents |