Clinical trial Recruiting at 1 site Observational Ages 18 and up

Monitoring and improving treatment for non-Hodgkin lymphoma patients in the Czech Republic

Official title: The Incidence, Epidemiology, Clinical Characteristic, Prognostic Factors, Therapy and Outcome of Non-Hodgkin Lymphoma Patients in the Czech Republic. NiHiL- Longitudinal Observational Study of Czech Lymphoma Study Group (CLSG)

Run by Czech Lymphoma Study Group · NCT03199066 · Data updated 2026-11-12

This study is trying to gather and analyze information about non-Hodgkin lymphoma patients in the Czech Republic to improve their diagnosis and treatment.

More Non Hodgkin Lymphoma (NHL) trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment20000 (estimated)
SponsorCzech Lymphoma Study Group
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Prague)
StatusRecruiting
StartedJanuary 1, 1999
Main results expectedDecember 31, 2020
Study endsDecember 31, 2027
Registry record updatedJune 26, 2017
Trial IDNCT03199066 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients diagnosed with non-Hodgkin lymphoma who are treated in the Czech Republic and can provide informed consent.

Probably not a fit

Patients under 18 years of age or those who do not provide signed informed consent 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

The Czech National Lymphoma Registry (NiHiL) aims to collect and analyze epidemiological data to enhance the diagnostic evaluation and treatment quality for patients with non-Hodgkin lymphoma (NHL). Patients are registered anonymously at diagnosis, and their data is updated throughout treatment and follow-up. The registry includes comprehensive information on lymphoma subtypes, treatment responses, and long-term outcomes, allowing for detailed analysis of survival rates and treatment efficacy. This initiative encompasses approximately 75% of NHL patients in the Czech Republic, providing a robust dataset for improving patient care.

Why it matters

Potential benefit: If successful, this registry could lead to improved treatment strategies and outcomes for patients with non-Hodgkin lymphoma.

How similar studies have gone: Other observational studies have shown success in improving treatment outcomes through comprehensive data collection, making this approach both validated and essential.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* lymphoma diagnosis
* treated in the Czech Republic
* signed informed consent

Exclusion Criteria:

* unsigned informed consent
* age \<18 y

Where it's running

  • Charles University General Hospital
    Prague, Czechia
    Recruiting

Study contacts

  • Principal investigator: Marek Trneny, prof. MD — Charles University General Hospital, Prague, CZ
  • Study coordinator: Marek Trneny, prof. MD
  • Email: trneny@cesnet.cz
  • Phone: +420224962061

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

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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.