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Dynamic Whole-body PET/CT Imaging in Clinical Oncology

Dynamic Whole-body PET/CT Imaging in Clinical Oncology

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06424873
Acronym
Dynamic PET/CT
Enrollment
60
Registered
2024-05-22
Start date
2024-04-01
Completion date
2025-12-31
Last updated
2024-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Brief summary

The goal of this clinical trial is to to achieve robust quantitative whole- body parametric imaging in clinically feasible scan times in patient with oncologic pathology . The main question\[s\] it aims to answer are: * \[question 1\] * \[question 2\] Participants will \[describe the main tasks participants will be asked to do, treatments they'll be given and use bullets if it is more than 2 items\].

Detailed description

Whole body hybrid PET/CT imaging, making use of the standardized uptake value (SUV), is well established in clinical setting for diagnosis and staging, treatment response monitoring and radiation therapy treatment planning of a wide range of oncologic malignancies. However, the SUV metric derived from static PET data does not capture the dynamics of the PET probe biodistribution in the body. The present work proposes to fill in this notable gap: namely to merge whole-body and dynamic PET/CT imaging, to achieve robust quantitative whole- body parametric imaging in clinically feasible scan times. Our proposed approach has the potential to significantly enhance diagnostic, prognostic and treatment response monitoring capabilities of PET/CT and to fundamentally alter routine clinical practice.

Interventions

RADIATIONPET/CT with FDG or FES

The study consists of an additional 50 minutes of imaging during the radiotracer's uptake phase prior to their clinical scan (standard of care).

Sponsors

Valentina Garibotto
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

PET/CT

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients clinically indicated for whole-body PET evaluation. 2. Patient must agree to lie still in the camera. 3. Patient must be able to comply with study procedures. 4. Patient must be able to provide informed consent.

Exclusion criteria

1. Patients \< 18 years of age. 2. Pregnant women are excluded.

Design outcomes

Primary

MeasureTime frameDescription
Standard SUV measurement metricthrough study completion , an average of 2 yearsThe standard SUV measurement metric will be compared with the measured influx rate Ki as obtained from dynamic PET/CT imaging for FDG-avid processes. We expect a correlation coefficient of at least 0.8.

Secondary

MeasureTime frameDescription
Image qualitythrough study completion , an average of 2 yearsThis will be assessed by clinical PET/CT readers, on a 5 point scale.
Certainty in diagnosis of FDG-avid processesthrough study completion , an average of 2 yearsThis will be assessed by clinical PET/CT readers, on a 5 point scale.

Countries

Switzerland

Contacts

Primary ContactValentina Garibotto, Pr
valentina.garibotto@hcuge.ch+41223727252
Backup ContactIsmini Mainta, Dr
IsminiCharis.Mainta@hcuge.ch+41795534454

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026