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TBPETCT001

Exploring new imaging opportunities using a large axial field of view PET-CT system

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Enrollment

Recruiting

No. of patients

12 evaluable patients

Population

Patients who have an indication for a standard FDG PET-CT scan

Design

This is a mono-center exploratory study to explore new imaging procedures with an ultra-high sensitivity total body PET-CT system

Key outcome parameters

The main endpoint for all sub-studies are assessment of the agreement in lesion detectability and quantitative standardized uptake values observed between new imaging procedures with those obtained using the routine clinical PET-CT imaging procedure and vendor recommended settings

Intervention

No interventions / treatments other than for routine patient care will be performed as part of this protocol

Key inclusion criteria

Inclusion criteria:

  • 18 years or older
  • Able to give consent
  • Signed informed consent
  • Patients who have an indication for a standard FDG PET-CT scan
  • For sub-study 2 (breath hold PET), patients with NSCLC, stage 2 or higher

Key exclusion criteria

Exclusion criteria:

  • Claustrophobic patients
  • Pregnant or breastfeeding woman
  • Uncontrolled diabetes mellitus
  • Any medical condition potentially hampering conduction of the study
  • Any other contraindication to undergo an FDG PET-CT examination

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