Clinical trial Recruiting at 1 site Observational Ages 18 and up

Observational study of lymphoma patients in Italy

Official title: Studio Osservazionale Retrospettivo Di Coorte Italiana Di Pazienti Con Linfoma (RETRO-LYMPH)

Run by IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06781437 · Data updated 2026-11-12

This study looks at lymphoma patients in Italy to see how different factors affect their treatment and survival over the years.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment5500 (estimated)
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna
Academic / other
Locations1 site (Bologna, Bologna)
StatusRecruiting
StartedFebruary 1, 2022
Main results expectedDecember 31, 2027
Study endsDecember 31, 2027
Registry record updatedJanuary 17, 2025
Trial IDNCT06781437 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals aged 18 and older who were diagnosed with lymphoma or lymphoproliferative syndrome between January 1980 and September 2021.

Probably not a fit

Patients who were diagnosed with lymphoma or lymphoproliferative syndrome outside the specified time frame will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study analyzes data from lymphoma patients diagnosed between January 1980 and September 2021 at a single center in Italy. It aims to identify clinical and epidemiological factors that influence disease progression and treatment outcomes. The study will also document various therapies, treatment durations, interruptions, and associated adverse events. By examining patient survival rates, the research seeks to enrich the understanding of lymphoma and lymphoproliferative syndromes for future studies.

Why it matters

Potential benefit: If successful, this study could provide valuable insights into the factors affecting lymphoma progression and treatment efficacy, potentially improving patient care.

How similar studies have gone: While observational studies on lymphoma exist, this specific retrospective approach focusing on a long time frame and detailed patient data is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age greater than or equal to 18 years of enrollment
* Diagnosis of lymphoma or lymphoproliferative syndrome between January 1980 and September 2021
* Signature of the informed consent form where applicable

Exclusion Criteria:

* none

Where it's running

  • IRCCS Azienda Ospedaliero - Universitaria di Bologna
    Bologna, Bologna, Italy
    Recruiting

Study contacts

  • Principal investigator: Pier Luigi Zinzani, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
  • Study coordinator: Pier Luigi Zinzani, MD
  • Email: pierluigi.zinzani@unibo.it
  • Phone: +390512143680

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.