Myocardial Blood Flow by PET and N-13 Ammonia During Regadenoson Stress

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by:
Mayo Clinic
ClinicalTrials.gov Identifier:
NCT01370265
First received: June 6, 2011
Last updated: February 14, 2012
Last verified: February 2012

June 6, 2011
February 14, 2012
February 2011
February 2012   (final data collection date for primary outcome measure)
Myocardial blood flow (MBF) [ Time Frame: 4 hours ] [ Designated as safety issue: No ]
To quantify regadenoson-induced hyperemic PET N-13 ammonia MBF and compare to adenosine-induced hyperemic PET N-13 ammonia MBF.
Same as current
Complete list of historical versions of study NCT01370265 on ClinicalTrials.gov Archive Site
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Myocardial Blood Flow by PET and N-13 Ammonia During Regadenoson Stress
Quantification of Myocardial Blood Flow by Positron Emission Tomography and N-13 Ammonia During Regadenoson Stress

The investigators propose to measure and compare regadenoson-induced hyperemic Myocardial Blood Flow (MBF) versus adenosine-induced hyperemic MBF, using PET N-13 Ammonia in healthy subjects. The protocol will provide clinically useful data for practice.

Growing clinical experience and published studies support the comparable diagnostic accuracy, safety, and better subjective tolerability of regadenoson as compared to adenosine. Furthermore, while dipyridamole and adenosine are contraindicated in patients with asthma and significant chronic obstructive pulmonary disease (COPD), pilot data suggest overall safety of regadenoson in patients with mild or moderate asthma and in patients with stable moderate COPD.

The use of the cyclotron-produced and FDA-approved PET perfusion tracer, N-13 ammonia, with regadenoson has not been published. Among the nuclear perfusion tracers, N-13 ammonia provides the best image quality, high diagnostic accuracy, and the lowest total body radiation exposure. Quantification of myocardial blood flow (MBF) in ml per min per gm is also possible with N-13 ammonia, adding clinically useful information and powerful prognostic value and is increasingly utilized in clinical practice. In studies of PET with N-13 ammonia, MBF increases up to four-fold with adenosine or dipyridamole in healthy human volunteers and normal myocardium. However, the PET acquisition protocol for N-13 ammonia with regadenoson stress and the limits of normal PET measured hyperemic blood flow after regadenoson infusion have not been published. The optimal timing of N-13 ammonia administration and of PET image acquisition as well as acquisition duration following regadenoson bolus is not known. Different physical and biological properties of PET perfusion tracers necessitate specific protocols for each tracer.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Regadenoson Stress
  • Drug: Regadenoson
    regadenoson (0.4 mg/5 ml IV) will be administered intravenously over 10 seconds, followed immediately by saline flush
    Other Name: Lexiscan
  • Drug: Adenosine
    adenosine (140 μg/kg/min) will be administered intravenously over 6 minutes
    Other Name: Adenoscan
  • Active Comparator: Regadenoson
    To Assess Regadenoson stress PET N-13 Ammonia MBF.
    Intervention: Drug: Regadenoson
  • Active Comparator: Adenosine
    To assess adenosine stress PET N-13 Ammonia MBF
    Intervention: Drug: Adenosine
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
12
June 2012
February 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Twelve healthy male and female volunteers over the age of 30.
  • Written informed consent will be obtained from each subject.
  • Each subject will undergo a history and physical examination

Exclusion Criteria:

  • Any cardiovascular or pulmonary symptoms or exam findings
  • History of low blood pressure (< 90/50 mmHg)
  • Prior cardiac history
  • History of hypertension
  • History of hyperlipidemia
  • History of diabetes mellitus
  • History of asthma or chronic obstructive pulmonary disease
  • Weight of > 450 pounds
  • Chronic kidney disease
  • Other serious illness such as cancer
  • Current smoking
  • Medication use (with the exception of acetaminophen, aspirin, NSAIDs, and thyroid hormone replacement)
  • Illicit drug use
  • Prior allergic reaction to adenosine, regadenoson, or aminophylline
  • Pregnancy
Both
30 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01370265
10-006377
No
Panithaya Chareonthaitawee M.D., Mayo Clinic
Mayo Clinic
Not Provided
Not Provided
Mayo Clinic
February 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP