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Taking people in ItalyNo phase

Whole body MRI scans in people with certain blood and cancer conditions

Studies whole body MRI scans in adults with lymphoma, prostate, breast, or myeloma conditions.

Plain-language title generated from the registry record
Registry title: Whole Body MRI in Oncology

Key facts

Where
Bologna, Meldola, and Milan, ItalySee the 3 sites

Where in Italy

  • IRCCS - Azienda Ospedaliero-Universitaria di Bologna - Policlinico di S. OrsolaBologna, ItalyTaking people
  • IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" - IRST S.r.l.Meldola, ItalyTaking people
  • IRCCS Istituto Europeo di Oncologia S.r.l.Milan, ItalyNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS
Trial code
NCT06895291
Record updated
30 March 2025
Original description
Multicenter, observational, prospective, study. All patients will be treated and monitored according to the local clinical practice. No additional procedures/patient visits in comparison with the usual clinical practice are planned for the study.Read full original descriptionShow less

Whole Body MRI in Oncology

Multicenter, observational, prospective, study. All patients will be treated and monitored according to the local clinical practice. No additional procedures/patient visits in comparison with the usual clinical practice are planned for the study.

Inclusion: Patients candidate to WB-MRI according to clinical practice belonging to the study groups listed above; Participant is willing and able to give informed consent for participation in the study; Male or Female, aged ≥ 18 years; Life expectancy greater than 3 months.

Exclusion: Patients with MRI-unsafe prostheses and devices; Patients whose tests are of suboptimal quality, or whose test has been suspended, or is incomplete.

ClinicalTrials.gov NCT06895291