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CompletedNCT00205166Updated Oct 29, 2012

Does Caffeine Affect the Sensitivity of Adenosine Perfusion Scans?

An interventional study of Cardiac SPECT imaging Rest and Stress and Caffeine in Coronary Artery Disease, sponsored by University of Wisconsin, Madison. Completed at 1 site in United States. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2012-10-29.

Sponsored by University of Wisconsin, Madison · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Coronary Artery Disease

Keywords

  • adenosine tracer scans
  • coronary artery disease
  • caffeine
03

In context

Coronary Artery Disease

5,598 studies on the registry are indexed under Coronary Artery Disease; 957 are open to participants now.

This study's enrollment of 50 is below the median of 124 across 3,436 interventional studies indexed under Coronary Artery Disease.

Browse Coronary Artery Disease studies →

Lead sponsor

University of Wisconsin, Madison is the lead sponsor of 1,161 studies on the registry; 182 are open to participants now.

Of its 151 completed or terminated interventional studies of FDA-regulated products, 114 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

Exclusion Criteria:

  • history of asthma, bronchospastic COPD, or renal failure
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (actual)

Study arms

  • Active comparator
    1

    Caffeine 400 mg PO 1 hour before adenosine infusion

    Procedure: Cardiac SPECT imaging Rest and Stress · Drug: Caffeine

  • Active comparator
    2

    Caffeine 200 mg po one hour before adenosine infusion

    Procedure: Cardiac SPECT imaging Rest and Stress · Drug: Caffeine

Interventions

  • ProcedureCardiac SPECT imaging Rest and Stress

    adenosine perfusion scintigraphy

  • DrugCaffeine

    Caffeine 400 mg po

  • DrugCaffeine

    Caffeine 200 mg po

06

What researchers measure

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

07

Study locations

1 site
  • University of Wisconsin
    Madison, Wisconsin 53792, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 29, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00205166
Lead sponsor
University of Wisconsin, Madison
Collaborators
Astellas Pharma US, Inc.
Responsible party
Sponsor
First posted
Sep 20, 2005
Start date
Jun 1999
Primary completion
Dec 2004
Completion
Dec 2004
Last update
Oct 29, 2012

Study contacts

Charles K Stone, MD
principal investigator · Univeristy of Wisconsin

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2012. You cannot join it, but the record below documents what was studied.

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