Myocardial Blood Flow by PET and N-13 Ammonia During Regadenoson Stress
| Tracking Information | |
|---|---|
| First Received Date ICMJE | June 6, 2011 |
| Last Updated Date | February 14, 2012 |
| Start Date ICMJE | February 2011 |
| Estimated Primary Completion Date | February 2012 (final data collection date for primary outcome measure) |
| Current Primary Outcome Measures ICMJE |
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. |
| Original Primary Outcome Measures ICMJE | Same as current |
| Change History | Complete list of historical versions of study NCT01370265 on ClinicalTrials.gov Archive Site |
| Current Secondary Outcome Measures ICMJE | Not Provided |
| Original Secondary Outcome Measures ICMJE | Not Provided |
| Current Other Outcome Measures ICMJE | Not Provided |
| Original Other Outcome Measures ICMJE | Not Provided |
| Descriptive Information | |
| Brief Title ICMJE | Myocardial Blood Flow by PET and N-13 Ammonia During Regadenoson Stress |
| Official Title ICMJE | Quantification of Myocardial Blood Flow by Positron Emission Tomography and N-13 Ammonia During Regadenoson Stress |
| Brief Summary | 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. |
| Detailed Description | 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. |
| Study Type ICMJE | Interventional |
| Study Phase | Not Provided |
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Crossover Assignment Masking: Open Label Primary Purpose: Diagnostic |
| Condition ICMJE | Regadenoson Stress |
| Intervention ICMJE |
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| Study Arm (s) |
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| Publications * | Not Provided |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |
| Recruitment Status ICMJE | Active, not recruiting |
| Estimated Enrollment ICMJE | 12 |
| Estimated Completion Date | June 2012 |
| Estimated Primary Completion Date | February 2012 (final data collection date for primary outcome measure) |
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both |
| Ages | 30 Years and older |
| Accepts Healthy Volunteers | Yes |
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects |
| Location Countries ICMJE | United States |
| Administrative Information | |
| NCT Number ICMJE | NCT01370265 |
| Other Study ID Numbers ICMJE | 10-006377 |
| Has Data Monitoring Committee | No |
| Responsible Party | Panithaya Chareonthaitawee M.D., Mayo Clinic |
| Study Sponsor ICMJE | Mayo Clinic |
| Collaborators ICMJE | Not Provided |
| Investigators ICMJE | Not Provided |
| Information Provided By | Mayo Clinic |
| Verification Date | February 2012 |
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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