Actively Recruiting

Age: 18Years +
All Genders
ID06781437

Retrospective Observational Study of Italian Cohort of Lymphoma Patients (RETRO-LYMPH)

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-17

5500

Participants Needed

1

Research Sites

308 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This observational, non-interventional, retrospective study focuses on patients diagnosed with lymphoma or lymphoproliferative syndrome between January 1980 and September 2021. The study aims to gather detailed clinical and epidemiological information to better understand factors influencing disease progression, including lifestyle, occupational factors, and treatment types. It also seeks to provide a foundation for future lymphoma research projects. The study reviews patient data from a single center over the specified time frame, describing the therapies used, treatment durations, reasons for treatment interruptions, patient responses, and any adverse events related to lymphoma treatments. It examines various outcomes such as progression-free survival, disease-free survival, and overall survival using statistical methods like Kaplan-Meier estimates. Participants will have their clinical histories analyzed, including survival and safety data related to their treatments. Researchers will perform descriptive analyses on patient characteristics and outcomes. The study involves an average follow-up period of six years, focusing on lymphoma incidence and prevalence within the center's patient population during the study period.

CONDITIONS

Official Title

Retrospective Observational Study of Italian Cohort of Lymphoma Patients (RETRO-LYMPH)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age greater than or equal to 18 years at enrollment
  • Diagnosis of lymphoma or lymphoproliferative syndrome between January 1980 and September 2021
  • Signature of the informed consent form where applicable
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

IRCCS Azienda Ospedaliero - Universitaria di Bologna

Bologna, Bologna, Italy, 40138

Actively Recruiting

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Research Team

P

Pier Luigi Zinzani, MD

A

Alessandro Broccoli, 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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