Retrospective Observational Study of Italian Cohort of Lymphoma Patients (RETRO-LYMPH)
RETRO-LYMPH
Studio Osservazionale Retrospettivo Di Coorte Italiana Di Pazienti Con Linfoma (RETRO-LYMPH)
1 other identifier
observational
5,500
1 country
1
Brief Summary
observational, non-interventional, retrospective, single-center study focusing on patients with lymphoma / lymphoproliferative syndrome between January 1980 and September 2021
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2022
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2022
CompletedFirst Submitted
Initial submission to the registry
December 3, 2024
CompletedFirst Posted
Study publicly available on registry
January 17, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2027
January 17, 2025
October 1, 2024
5.9 years
December 3, 2024
January 13, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Incidence and prevalence of lymphomas/lymphoproliferative syndromes referred to the Centre between January 1980 and September 2021
Incidence and prevalence
through study completion, an average of 6 years
Secondary Outcomes (12)
Overall Survival (OS)
through study completion, an average of 6 years
event free survival (EFS)
through study completion, an average of 6 years
Lymphoma specific survival (LSS)
through study completion, an average of 6 years
Progression Free Survival (PFS)
through study completion, an average of 6 years
Net survival (5 years)
through study completion, an average of 6 years
- +7 more secondary outcomes
Eligibility Criteria
Patients with lymphoma / lymphoproliferative syndrome between January 1980 and September 2021
You may qualify if:
- 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
You may not qualify if:
- none
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
IRCCS Azienda Ospedaliero - Universitaria di Bologna
Bologna, Bologna, 40138, Italy
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Pier Luigi Zinzani, MD
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 3, 2024
First Posted
January 17, 2025
Study Start
February 1, 2022
Primary Completion (Estimated)
December 31, 2027
Study Completion (Estimated)
December 31, 2027
Last Updated
January 17, 2025
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will not share