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Taking people in GermanyNo phase

Studies a PSMA-1007 scan to find prostate cancer that has returned after treatment

Tests a PSMA-1007 imaging scan in adults whose prostate cancer has returned after treatment.

Plain-language title generated from the registry record
Registry title: Diagnostic Performance of [18F]PSMA-1007 in the Context of Biochemical Recurrence of Prostate Cancer

Key facts

Where
Düsseldorf, GermanySee the site

Where in Germany

  • Department of Nuclear Medicine, Medical Faculty and University Hospital Duesseldorf, Heinrich-Heine-University DuesseldorfDüsseldorf, GermanyTaking people

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Trial details

Who runs it
Heinrich-Heine University, Duesseldorf
Trial code
NCT06657131
Record updated
17 January 2025
Original description
Following numerous retrospective studies and Phase-3-Studies with promising results, [18F]PSMA-1007 has been approved by european authorities. Therefore, it is a growing deployment of this diagnostic method anticipated. This study aims to investigate the diagnostic performance and clinical impact in a real-world-evidence in the context of regular clinical care. The evidence generated by this approach is supposed to assist in optimizing the management of prostate cancer patients.Read full original descriptionShow less

Diagnostic Performance and Clinical Impact of [18F]PSMA-1007 in the Context of Biochemical Recurrence of Prostate Cancer: a Real-World Evidence from a Monocentric, Prospective Observational Phase-4-Trial

Following numerous retrospective studies and Phase-3-Studies with promising results, [18F]PSMA-1007 has been approved by european authorities. Therefore, it is a growing deployment of this diagnostic method anticipated. This study aims to investigate the diagnostic performance and clinical impact in a real-world-evidence in the context of regular clinical care. The evidence generated by this approach is supposed to assist in optimizing the management of prostate cancer patients.

Inclusion: Informed Consent; Conduct of [18F]PSMA-1007 PET Imaging in the context of regular clinical care.

Exclusion: Technical Flaws in the acquisition protocol.

ClinicalTrials.gov NCT06657131