Status:

COMPLETED

The MATCH Investigation: CT Myocardial Perfusion and CT-FFR vs PET MPI

Lead Sponsor:

Emory University

Collaborating Sponsors:

Siemens Medical Solutions

Conditions:

Coronary Artery Disease

Eligibility:

All Genders

18-85 years

Phase:

NA

Brief Summary

The overall goal of this project is to compare the absolute quantification of myocardial perfusion done by using CT myocardial perfusion imaging (CT-MPI) and the coronary flow measured by using CT Fra...

Detailed Description

Participants will be patients who are scheduled to undergo PET Myocardial Perfusion Imaging, which is the traditional method for evaluating patients with suspected blockages or narrowing of the heart ...

Eligibility Criteria

Inclusion

  • Referred for a clinically indicated CT-MPI for CAD assessment
  • Must provide written informed consent prior to any study-related procedures being performed
  • Must be willing to comply with all clinical study procedures

Exclusion

  • Pregnant or nursing females. The possibility of pregnancy will be excluded by testing (serum or urine ßHCG) within 24 hours before study agent administration, or if the woman has previous surgical sterilization, or if the woman is post-menopausal, with minimum one (1) year history without menses.
  • Currently taking or has taken within 48 hours the following excluded medications:
  • ActoPlus Met (Pioglitazone + metformin)
  • Avandamet (Rosiglitazone + metformin)
  • Fortamet (metformin)
  • Glucovance (Glyburide +metformin)
  • Glucophage (metformin)
  • Glucophage extended-release (XR) (metformin)
  • Glumetza (metformin)
  • Janumet (Sitagliptin + metformin)
  • Metformin
  • Metaglip (Glipizide + metformin)
  • Riomet (metformin)
  • Acute psychiatric disorder
  • Unwilling to comply with the requirements of the protocol
  • Previously entered this study
  • Known hypersensitivity to iodinated contrast material, beta-blockers, or pharmaceutical stressors used in this study
  • Suffers from claustrophobia
  • Impaired renal function (GFR \< 45 ml/min)
  • Acute hypotension (\<100 mm Hg systolic)
  • 2nd or 3rd degree atrioventricular (AV) block

Key Trial Info

Start Date :

June 16 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 24 2024

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT04316676

Start Date

June 16 2021

End Date

September 24 2024

Last Update

January 6 2026

Active Locations (1)

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1

Emory University Hospital

Atlanta, Georgia, United States, 30322