Clinical trial · Interventional
Dynamic Whole-body PET/CT Imaging in Clinical Oncology
NCT06424873CI-TRIAL-00077377Dynamic PET/CTunknownN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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 \[describe the main tasks participants will be asked to do, treatments they'll be given and use bullets if it is more than 2 items\].
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| PET/CT with FDG or FES | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- One arm study
- description
- Additionnal images during PET/CT
- interventionNames
- Radiation: PET/CT with FDG or FES
Primary outcomes (1)
- measure
- Standard SUV measurement metric
- timeFrame
- through study completion , an average of 2 years
- description
- The 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 outcomes (2)
- measure
- Image quality
- timeFrame
- through study completion , an average of 2 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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.
References
Publications (0)
Data not yet available
No reference posted for this study.