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.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 20000 (estimated) |
| Sponsor | Czech Lymphoma Study Group Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Prague) |
| Status | Recruiting |
| Started | January 1, 1999 |
| Main results expected | December 31, 2020 |
| Study ends | December 31, 2027 |
| Registry record updated | June 26, 2017 |
| Trial ID | NCT03199066 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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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.