Fact CheckerSign in

NCT07746232Not yet recruiting

Validating DW-MRI and Fat Fraction in Multiple Myeloma Post-ASCT: The RAC-FAT Study"

Multicenter Observational Study for the Validation of the Predictive Role of Diffusion-Weighted Whole-body MRI (DW-MRI) Imaging Response According to MY-RADS Criteria (RAC Score) and Fat Fraction (rFF%) After Autologous Stem Cell Transplantation in Multiple Myeloma Patients Treated With First-Line Anti-CD38-Based Therapy (RAC-FAT Study)

Source: ClinicalTrials.gov · Last updated 9 Sept 2026

Brief summary (registry, in English)

This is a multicenter, observational, retrospective-prospective study designed to validate the predictive role of advanced imaging in patients with newly diagnosed multiple myeloma (NDMM). The main purpose of this study is to estimate the prevalence of radiological response categories (Response Assessment Category, RAC score) and evaluate the predictive value of relative Fat Fraction (rFF%) using Diffusion-Weighted Whole-Body Magnetic Resonance Imaging (DW-MRI) in patients who have undergone autologous stem cell transplantation (ASCT) after receiving first-line anti-CD38-based quadruplet induction therapy.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
92 (estimated)
First submitted
21 Jul 2026
Start date
1 Oct 2026
Primary completion date
31 Aug 2028
Lead sponsor
Fondazione EMN Italy Onlus
NCT number
NCT07746232

What you commit to

  • Study type: Observational
  • Planned participants: 92
  • From 1 Oct 2026 to the primary completion date, 31 Aug 2028
  • 10 sites 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

  • \- Absence of post-ASCT/pre-maintenance DW-MRI.

Who the study is looking for

  • Newly diagnosed MM participants eligible for ASCT, treated with anti-CD38-based quadruplet induction therapy and ASCT, with post-ASCT/premaintenance DW-MRI available (in tandem ASCT, DW-MRI after second ASCT will be considered).
  • Age ≥18 years.
  • Participant must sign an informed consent form (ICF) that he or she understands the purpose of, and procedures required for the trial and is willing to participate in the trial.

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

Full criteria on ClinicalTrials.gov

Sites (10)

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

SiteCityCountrySite status
IRCCS Istituto Tumori "G. Paolo II - U.O.C. Ematologia e Terapia Cellulare
Coordinator of this site? Confirm its status
BariItalyUnknown status
A.O.U. di Bologna Policlinico S.Orsola Malpighi
Coordinator of this site? Confirm its status
BolognaItalyUnknown status
A.O. Spedali Civili di Brescia
Coordinator of this site? Confirm its status
BresciaItalyUnknown status
Istituto Oncologico Veneto IRCCS - UOC Oncoematologia
Coordinator of this site? Confirm its status
Castelfranco VenetoItalyUnknown status
Ospedale Classificato Valduce
Coordinator of this site? Confirm its status
ComoItalyUnknown status
Ospedale Niguarda
Coordinator of this site? Confirm its status
MilanItalyUnknown status
I.R.C.C.S. Ospedale S. Raffaele
Coordinator of this site? Confirm its status
MilanItalyUnknown status
A.O.U. Maggiore della Carità
Coordinator of this site? Confirm its status
NovaraItalyUnknown status
Policlinico S. Matteo Fondazione IRCCS
Coordinator of this site? Confirm its status
PaviaItalyUnknown status
ASL Roma 1
Coordinator of this site? Confirm its status
RomeItalyUnknown status

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