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Clinical Trials/NL-OMON45317
NL-OMON45317
Completed
Phase 3

Prostate Cancer Imaging with [18Flourine]Prostate Specific Membrane Antigen (PSMA) PET: a study on pharmacokinetics and test repeatability - Pharmacokinetics and repeatability of [18F]PSMA

Vrije Universiteit Medisch Centrum0 sites20 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
prostate cancer
Sponsor
Vrije Universiteit Medisch Centrum
Enrollment
20
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • \- Histologically proven prostate cancer, with lymphatic and/or haematogeneous metastases;
  • \- Written informed consent;
  • \- At least 2 metastases in the thorax per patient detected by conventional imaging (e.g., bone scan, either CT or MRI of the chest, abdomen and pelvis); conventional imaging should be recently performed (no longer than 3 months previous to the PET\-CT scan);
  • \- At least one tumour (metastasis) with diameter \* 1\.5 cm (to minimize partial volume effects);
  • \- Patients able to remain supine for 60 minutes in the PET\-CT scanner;;Part B;
  • \- Histologically proven prostate cancer, with lymphatic and/or haematogeneous metastases;
  • \- Written informed consent;
  • \- At least one tumour (metastasis) with diameter \>1\.5 cm detected by recently performed conventional imaging (maximal 3 months prior to the PET\-CT scan);
  • \- Patients able to remain supine for 80 minutes in the PET\-CT scanner;

Exclusion Criteria

  • A potential subject who meets any of the following criteria will be excluded from participation in this study:
  • \- Claustrophobia (part A and B);
  • \- Multiple malignancies (part A and B);
  • \- Participation part A (Part B)

Outcomes

Primary Outcomes

Not specified

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