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OpenTrials
Completed

NCT Number: NCT00205166

Does Caffeine Affect the Sensitivity of Adenosine Perfusion Scans?

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Wisconsin

Madison, Wisconsin, 53792, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who have already completed rest/stress 99mTc sestamibi or 99mTc tetrofosmin imaging will be given a form describing this protocol and asked to volunteer for the additional scan

Exclusion criteria

  • history of asthma, bronchospastic COPD, or renal failure

Treatment and study plan

Cardiac SPECT imaging Rest and Stress

Procedure

adenosine perfusion scintigraphy

Caffeine

Drug

Caffeine 400 mg po

Primary outcomes

  1. This protocol has a specific aim of determining whether prior caffeine administration affects the sensitivity and specificity of adenosine perfusion scintigraphy for detection of impaired coronary vascular reserve.

    Time frame: Assessment is made at the time of research adenosine perfusion scintigraphy

Secondary outcomes

  1. determination of caffeine levels in patients instructed to hold caffeine prior to adenosine imaging

    Time frame: Assess at time of lab sample results obtained

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Collaborators

  • Astellas Pharma US, Inc.

Registry information

Important dates

Study start
1999
Primary completion
2004
Study completion
2004
First posted
Sep 20, 2005
Registry last updated
Oct 29, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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