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Ga-68-NODAGA-MJ9 Compared to F-18-FCH PET/CT for Prostate Cancer Patients

L

Lausanne University Hospital (CHUV)

Status

Completed

Conditions

Prostate Cancer

Treatments

Diagnostic Test: 1 PET/CT with F-18-FCH + 1 PET/CT with Ga-68-NODAGA-MJ9

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Prostate cancer patients for whom a F-18-FCH PET/CT is indicated. Ga-68-NODAGA-MJ9 is a new PET/CT radiotracer aiming at giving complementary information : more precise images and early localisation of recurrence to standard imaging

Full description

Patient with primary or relapsing prostate cancer for whom F-18-FCH PET/CT is indicated will be proposed to participate to the present study. After signing the patient informed consent, both F-18-FCH and Ga-68-NODAGA-MJ9 PET/CT will be scheduled with a maximum 10 day-interval.

No adverse events are expected.

Enrollment

60 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age : adult patients
  • Karnofsky : ≥ 80%
  • Patients with histologically proven prostate cancer for whom 18F-fluocholine PET/CT is indicated for primary cancer staging, or for recurrence with increase of blood PSA. In order to provide a detection probability of 30% or more, a blood PSA 0.5 ng / ml or more in post initial curative intent surgery will be required.
  • Signed informed consent.

Exclusion criteria

  • Lack of discernment to sign the consent form
  • Age <18 years
  • Patient under hormonal treatment

Trial design

60 participants in 1 patient group

F-18-FCH & Ga-68-NODAGA-MJ9
Description:
1 PET/CT with F-18-FCH + 1 PET/CT with Ga-68-NODAGA-MJ9
Treatment:
Diagnostic Test: 1 PET/CT with F-18-FCH + 1 PET/CT with Ga-68-NODAGA-MJ9

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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