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NCT06460454Completed

PROnostic Interest of 18F-FDG PET/CT in Patients With Metastatic Castration-resistant Prostate Cancer (mCPRC) Progressing

PROnostic Interest of 18F-FDG PET/CT in Patients With Metastatic Castration-resistant Prostate Cancer (mCPRC) Progressing on Chemotherapy, Treated With 177 Lu-PSMA (PROFLu)D7 (± 1 Day)

Source: ClinicalTrials.gov · Last updated 4 Mar 2025

Brief summary (registry, in English)

The aim of this retrospective study was to assess the prognostic value of parameters extracted from 18FDG PET/CT and 68Ga-PSMA PET in the initial workup and follow-up of patients treated with 177Lu-PSMA in mCRPC.

Status (registry)
Completed
Study type
Observational
Enrollment
100 (actual)
First submitted
11 Jun 2024
Start date
1 Nov 2024
Primary completion date
1 Jan 2025
Lead sponsor
Central Hospital, Nancy, France
NCT number
NCT06460454

What you commit to

  • Study type: Observational
  • Participants enrolled: 100
  • From 1 Nov 2024 to the primary completion date, 1 Jan 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients who did not give their consent to use their data retrospectively

Who the study is looking for

  • Patients treated with 177Lu-PSMA for castration-resistant prostate cancer at Nancy University Hospital
  • Patients with 68Ga-PSMA and 18FDG PET scans as part of the initial workup and treatment follow-up

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Nuclear medicine Department CHRU de NANCY
Coordinator of this site? Confirm its status
Vandœuvre-lès-NancyFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.