Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Can CZT-SPECT/CT quantify myocardial tracer uptake to match PET measurements in coronary artery disease?

Official title: Quantitative Myocardial Perfusion Imaging Assessment by SPECT/CT: Evaluation of Standardized Uptake Value (SUV) and Correlation With Myocardial Flow Reserve (MFR) Assessed by PET/CT

Run by Centre Hospitalier Régional d'Orléans · NCT07708805 · Data updated 2026-11-12

This study tests whether CZT-SPECT/CT can quantify heart blood flow at rest and stress and see if the results align with PET measurements for people with coronary artery disease.

More Coronary Artery Disease trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorCentre Hospitalier Régional d'Orléans
Academic / other
Locations1 site (Orléans, Loiret)
StatusRecruiting
StartedSeptember 21, 2026
Main results expectedSeptember 25, 2027
Study endsNovember 25, 2027
Registry record updatedOctober 13, 2026
Trial IDNCT07708805 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) with suspected or known coronary artery disease referred for functional imaging after prior coronary angiography showing non-significant to moderate disease.

Probably not a fit

Patients with severe coronary disease needing immediate revascularization or a history of prior revascularization may not benefit from this approach.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This exploratory study evaluates if newer CZT-SPECT/CT cameras can provide absolute quantification of myocardial tracer uptake, using standardized uptake values, during rest and stress. Primary goal is to compare stress-to-rest SUV ratios from SPECT with myocardial flow reserve from PET imaging. Participants are adults with suspected or known coronary disease referred for functional cardiac imaging after prior angiography showing non-obstructive to moderate disease. The study uses stress and rest SPECT/CT imaging to assess feasibility of substituting or supplementing PET-based quantification. The investigation is conducted at a single center in Orléans, with eligibility criteria focusing on those without severe disease or prior revascularization and adequate imaging compatibility.

Why it matters

Potential benefit: If successful, patients could gain access to a more readily available and potentially lower-cost quantification method for myocardial perfusion.

How similar studies have gone: Previous PET-based quantification is established; CZT-SPECT/CT quantification is exploratory and feasibility-focused, with limited prior demonstration of equivalent accuracy.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Participant has provided informed consent to participate in the study.
2. Age ≥ 18 years.
3. Patients referred for functional cardiac imaging assessment (SPECT or PET) following diagnostic coronary CT angiography (CCTA) or invasive coronary angiography demonstrating either:

   * moderate coronary atherosclerosis without significant coronary stenosis (\<50% stenosis), or
   * coronary lesions for which functional cardiac imaging assessment or medical therapy is indicated.

Exclusion Criteria:

1. Severe coronary artery disease requiring prompt revascularization by percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG), including left main coronary artery stenosis \>50% or other severe coronary lesions with FFR \<0.80.
2. History of coronary revascularization (PCI, coronary stenting, or CABG).
3. Left ventricular ejection fraction (LVEF) \<35%.
4. Contraindication to pharmacological stress testing for cardiac PET/SPECT, including severe hypotension, second- or third-degree atrioventricular block, or recent myocardial infarction.
5. Protected adult under legal guardianship or curatorship.
6. Individual under judicial protection measures.
7. Individual deprived of liberty.
8. Individual not affiliated with a health insurance
9. Pregnant or breastfeeding woman.

Where it's running

  • Centre Hospitalier Universitaire d'Orléans
    Orléans, Loiret, France
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.