Actively Recruiting
A Comprehensive Register Of Lymphoproliferative Disorders (ReLy)
Led by Fondazione IRCCS Policlinico San Matteo di Pavia · Updated on 2026-04-09
9000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This observational study focuses on patients aged 18 and older who have lymphoproliferative disorders, a group of blood cancers affecting the lymphatic system. Researchers aim to understand the overall survival over 10 years for different types of these disorders. The study also examines factors like patient fitness, comorbid conditions, and how these influence treatment choices and outcomes. New therapies including chemo-free protocols, targeted drugs, and cell therapies are being evaluated to determine the best treatment sequences for cases that are refractory or relapsed. Participants will be observed through various phases of their disease, including diagnosis and treatment stages. The study investigates the impact of clinical and biological factors on disease progression or relapse, as well as potential links between genetic profiles and clinical outcomes. It also monitors adverse events like tumor lysis syndrome and their effects on treatment adjustments. Additionally, the study looks at patients managed with a watch-and-wait approach, long-term toxicities, secondary cancers, and healthcare resource use. Throughout the study, participants' health and treatment outcomes will be regularly assessed using clinical data collected from diagnosis through follow-up. Researchers will analyze survival rates, treatment effectiveness, and side effects over a long period from 2002 to 2030. This comprehensive data collection aims to improve understanding of lymphoproliferative disorders and optimize patient management strategies over time.
CONDITIONS
Brief Title
A Comprehensive Register Of Lymphoproliferative Disorders (ReLy)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years or older diagnosed with or treated for lymphoproliferative disorders.
- Prospective patients or their legal guardians able to understand and willing to sign a written informed consent document.
- Retrospective patients who have signed the institutional document allowing use of their data for research.
You will not qualify if you...
- Patients unable to understand the informed consent document.
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.
1 visit (in-person)
Duration - Up to 28 years
Participants are observed over time to evaluate overall survival and disease progression of lymphoproliferative disorders.
Periodic visits based on clinical follow-up and data collection schedules
Trial Site Locations
Total: 1 location
1
Fondazione IRCCS Policlinico San Matteo
Pavia, Lombardy, Italy, 27100
Actively Recruiting
Research Team
L
Luca Arcaini
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
5
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