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NCT06321679Recruiting

Response Evaluation of Cancer Therapeutics in Metastatic Castration-Resistant Prostate Cancer to the Bone

Response Evaluation of Cancer Therapeutics in Metastatic Castration-Resistant Prostate Cancer (mCRPC) to the Bone: A Whole Body MRI Study

Source: ClinicalTrials.gov · Last updated 20 Mar 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study is aimed to compare whole body MRI (WB-MRI) with Bone Scintigraphy (BS) and Computerized Tomography (CT) scans in patients receiving treatment for metastatic castration-resistant prostate cancer to the bone. This is a monocentric, prospective observational study.

Status (registry)
Recruiting
Study type
Observational
Enrollment
40 (estimated)
First submitted
13 Mar 2024
Start date
3 Jul 2020
Primary completion date
31 Dec 2024
Lead sponsor
European Institute of Oncology
NCT number
NCT06321679

What you commit to

  • Study type: Observational
  • Planned participants: 40
  • From 3 Jul 2020 to the primary completion date, 31 Dec 2024
  • 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 illness

  • Radical treatment of sole site of metastatic disease (e.g. Cyberknife to solitary metastatic lesion),
  • Psychological, familial, sociological or geographical conditions that would hamper compliance with the study protocol; such conditions are to be discussed with the patient as part of the informed consent process.

Other

  • Absolute contraindication to WB-MRI, CT or BS,

Who the study is looking for

  • Histological diagnosis of castration-resistant prostate cancer,
  • Single or multiple bone metastases,
  • Life expectancy of over 6 months,
  • No current active malignancy other than prostate cancer,
  • Provision of written informed consent.

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

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
IEO Istituto Europeo di Oncologia
Coordinator of this site? Confirm its status
MilanItalyRecruiting

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