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Quantification of Myocardial Blood Flow by Positron Emission Tomography in Healthy Volunteers (PET Normals)

O

Ochsner Health System

Status

Unknown

Conditions

Normal Healthy Volunteers Without Chronic Medical Conditions

Treatments

Procedure: cardiac PET stress test

Study type

Observational

Funder types

Other

Identifiers

NCT03895554
STUDY00000188

Details and patient eligibility

About

To establish quantitative values of myocardial blood flow (MBF) in normal, healthy volunteers .

Full description

We seek to establish quantitative values of myocardial blood flow in 20 normal, healthy volunteers using our existing 2D PET camera (Positron Attrius) and invasively validated software package (HeartSee) in order to 1) establish institutional values for which clinical patients can be compared to and 2) add to the collective data of the scientific community. Values to be measured will be resting myocardial blood flow (MBF), stress MBF and coronary flow reserve.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults ≥18 and <40 years old
  • Participants must be able to give informed consent.
  • Ability to abstain from caffeine for 48 hours

Exclusion criteria

  • Any chronic cardiac disease or condition (e.g. hypertension, hyperlipidemia)
  • Any chronic systemic disease or condition (e.g. diabetes, systemic lupus, rheumatoid arthritis)
  • Tobacco use
  • Family history in a first degree relative with clinical coronary artery disease (history of myocardial infarctio, percutaneous intervention or coronary artery bypass grafting) in men <55 years old or women <65 years old
  • Severe claustrophobia
  • Positive urine pregnancy test
  • Inability to give informed consent

Trial design

20 participants in 1 patient group

Normal volunteers
Description:
Normal, healthy volunteers with undergo cardiac PET stress testing.
Treatment:
Procedure: cardiac PET stress test

Trial contacts and locations

1

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Central trial contact

Hunter McDaniel; Robert M Bober, MD

Data sourced from clinicaltrials.gov

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