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Dynamic FDG PET/CT: Optimization and Validation of Data Acquisition (VALIDATE)

A

Aarhus University Hospital

Status

Completed

Conditions

Positron-Emission Tomography

Treatments

Diagnostic Test: Dynamic Whole-Body parametric PET/CT

Study type

Interventional

Funder types

Other

Identifiers

NCT04660279
AarhusUH

Details and patient eligibility

About

Quantification of the metabolic rate of glucose from Dynamic Whole-Body PET examinations requires measurements of the time course of the radioactivity concentrations in arterial blood by blood sampling, and in the tissue of interest by dynamic PET. Invasive arterial blood sampling cannot be part of a standard examination, and therefore the blood samples need to be replaced by activity concentrations derived from the PET images, usually from small volumes in the descending aorta or left ventricle.

Newly developed scanner software (Siemens) allows automated CT-based identification of blood pool regions and extraction of an image-derived blood input function from the corresponding PET data.

However, this automated method needs validation, as it could be prone to systematic errors caused by limited spatial resolution, patient movement, and image reconstruction. We will use invasively measured arterial blood samples as a reference for validation of methods to extract non-invasive PET image-derived input functions and quantify any systematic errors that could propagate to the resulting parametric images.

Enrollment

20 patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with a planned clinical standard PET/CT as part of pre-therapeutic staging, response assessment scanning.
  • Good performance status, which will allow us to obtain informed consent to draw the required arterial blood samples during the examination, and which will permit patients to lay still in the scanner for at least 70 min.

Exclusion criteria

  • • Age < 18 or > 85 years

    • Patients that can not tolerate a PET scan (f.ex: claustrophobia).

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Validate
Other group
Description:
D-WB PET/CT scans + arterial blood sampling.
Treatment:
Diagnostic Test: Dynamic Whole-Body parametric PET/CT

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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