Actively Recruiting
Anonymization of Clinical Data From Pseudonymized Databases Collected as Part of Previous Clinical Trials on Multiple Myeloma
Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2026-05-12
600
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research investigates multiple myeloma by analyzing previously collected genomic, clinical, and imaging data from past studies conducted at the Hematology Unit of IRCCS Azienda Ospedaliero-Universitaria di Bologna. The goal is to understand how these different types of information relate to disease outcomes and to create predictive models using artificial intelligence and machine learning that might forecast disease progression and treatment responses in the future. The study uses existing, pseudonymized data without requiring any new tests, procedures, or patient visits. The data includes genomic profiles from bone marrow and blood samples and imaging to describe disease distribution at baseline. Secondary measures will assess treatment response and early relapse within 18 months of therapy start. Participants are not actively involved since the study is retrospective and observational. Researchers will securely develop and store anonymized datasets for analysis. The main outcomes include detailed genomic descriptions and imaging data at baseline, with follow-up on therapy response and relapse rates. The study is planned to run until 2028.
CONDITIONS
Brief Title
Anonymization of Clinical Data From Pseudonymized Databases Collected as Part of Previus Clinical Trials on Multiple Myeloma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Signed informed consent
- Confirmed diagnosis of multiple myeloma
- Previously enrolled in a spontaneous trial at the Hematology Unit of IRCCS AOU di Bologna since 2021 with pseudonymized datasets available
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 6 years
Participants who underwent previous clinical trials are observed through analysis of anonymized clinical data collected from pseudonymized databases.
Trial Site Locations
Total: 1 location
1
IRCCS AOU Policlinico Sant'Orsola
Bologna, Bo, Italy, 40138
Actively Recruiting
Research Team
C
Carolina Terragna, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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