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Verification of Imaging System PCD-1000A

C

Canon

Status

Completed

Conditions

Cancer Patients

Treatments

Device: PET/CT imaging

Study type

Observational

Funder types

Industry

Identifiers

NCT04024748
PCD-1000A

Details and patient eligibility

About

Scope Verification of technologies included in the PCD-1000A PET/CT imaging chain.

  • Define and confirm all supported clinical protocols
  • Evaluate performance

Full description

The study aim is system verification and associated software. Clinical data and clinical feedback will be used for verification.

Enrollment

24 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients already scheduled for an FDG test at SDMI
  • 40 years and older
  • Capable of providing their informed consent

Exclusion criteria

  • Patients not scheduled for an FDG test at SDMI
  • 39 years or younger
  • Adult female patients that are and/or could become pregnant
  • Not capable of providing their informed consent

Trial design

24 participants in 1 patient group

Patients already scheduled for a FDG test
Description:
Subjects will be selected from patients already scheduled for a routine FDG PET/CT test. Only adult patients, 40 years old or older, capable of providing their informed consent, will be selected. Any adult female patients that are pregnant and/or could become pregnant will be excluded. Twenty patients will be recruited.
Treatment:
Device: PET/CT imaging

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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