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Active Not RecruitingNCT02562131

PET-MR-PSA Prostate Cancer Recidive Study

18F-Fluciclovine PET/MRI for Detection of Recurrent Prostate Cancer After Radical Treatment

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
80 (actual)
Sponsor
Norwegian University of Science and Technology · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

Simultaneous PET/MRI has the potential to improve the detection accuracy in recurrent prostate cancer, since it combines the excellent soft-tissue contrast of MRI with the high molecular sensitivity of PET in a single imaging session. The aim of this study is to evaluate the sensitivity and specificity of simultaneous 18F-Fluciclovine PET/MRI for detection of recurrent prostate cancer.

Detailed description

The patients follow standard treatment and follow-up after the PET/MRI exam, which will be determined by the patient's treating urologist and/or oncologist. Data from histopathology, clinical follow-up and follow-up imaging will be collected to establish a reference standard that defines the presence or absence of disease for each patient. The imaging findings will be compared with the reference standard to assess the sensitivity and specificity. The diagnostic accuracy of combined PET/MRI and MRI-only (the current clinical standard) will be compared.

Conditions

Timeline

Start date
2015-09-01
Primary completion
2027-12-01
Completion
2027-12-01
First posted
2015-09-29
Last updated
2025-06-06

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT02562131. Inclusion in this directory is not an endorsement.