Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
1500 participants
OBSERVATIONAL
2021-12-07
2026-08-31
Brief Summary
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Detailed Description
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Study-specific questionnaires will be administered to patients, both at baseline and during follow-up, which methodologically represent a useful tool in order to achieve these objectives.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Diagnosis of lymphoma within 3 months of enrollment
* Patients may have been treated, as long as the initial diagnosis of lymphoma is within 3 months of enrollment
* Signing of the informed consent form
Exclusion Criteria
18 Years
ALL
No
Sponsors
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IRCCS Azienda Ospedaliero-Universitaria di Bologna
OTHER
Responsible Party
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Principal Investigators
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Pier Luigi Zinzani, MD
Role: PRINCIPAL_INVESTIGATOR
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Locations
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IRCCS Azienda Ospedaliero - Universitaria di Bologna
Bologna, Bologna, Italy
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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LYMPH-OS
Identifier Type: -
Identifier Source: org_study_id
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