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A Registry Study on HIV-related Lymphoma

Sponsor: Rotkreuzklinikum München gGmbH

NCT ID: NCT05231135

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 96 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor

In plain English

This registry study collects information about people who have lymphoma (a cancer of the immune system) and human immunodeficiency virus (HIV) at the same time. A registry study gathers health records over time to learn more about these conditions. The sponsor is Rotkreuzklinikum München gGmbH.

Who can take part

  • Lymphoma confirmed by tissue or cell tests (non-Hodgkin or Hodgkin lymphoma)
  • HIV infection at the time the lymphoma was found
  • Lymphoma diagnosed since 1 January 2010
  • Adults aged 18 or over
  • Written informed consent given

Who may not be able to

  • HIV diagnosed more than 3 months after the lymphoma diagnosis
  • Not able or willing to attend follow-up (for the forward-looking part of the study)

What taking part involves

  • • Not stated — ask the trial team. This is a registry study, so it may only involve collecting your existing health information.

Time commitment: Not stated — ask the trial team about visits, duration, and what taking part involves.

Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.

Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
300
Started
2021-08-25
Last checked
2023-04

Plain English Summary

What is this study?

  • • Testing a new treatment for aids related lymphoma
  • • Clinical study - 300 participants
  • • Retrospective und prospective registry on HIV-associated lymphoma

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with aids related lymphoma

Where?

  • • Cardiff - University Hospital of Wales

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Retrospective und prospective registry on HIV-associated lymphoma. Data on characteristics, type and toxicity of treatment and outcome of patients with HIV-lymphoma will be collected.

More detail

To study characteristics, treatment approaches and outcome of HIV-infected patients with malignant lymphoma in the combination antiretroviral therapy (cART) era. HIV-infected persons diagnosed with non-Hodgkin lymphoma or Hodgkin lymphoma will be included. The choice of treatment is not specified by the registry study. However, the type of antineoplastic treatment should follow national or international recommendations and guidelines. Data will be pseudonymized by the data manager of the treating institution. Central data management is located at Red Cross Hospital Munich, Germany.

AIDS Related LymphomaHIV Related Lymphoma

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Histology or cytology proven non-Hodgkin lymphoma or Hodgkin lymphoma
  • ✓HIV-infection at time of lymphoma diagnosis
  • ✓Lymphoma diagnosis since 01.01.2010
  • ✓Adult patients ≥ 18 years
  • ✓Written agreement to take part

Who cannot take part

  • ✗HIV-diagnosis \> 3 months after the diagnosis of malignant lymphoma
  • ✗Non-Compliance or lack of opportunity for follow-up (for the prospective part of the study)
See the full criteria
Inclusion Criteria: * Histology or cytology proven non-Hodgkin lymphoma or Hodgkin lymphoma * HIV-infection at time of lymphoma diagnosis * Lymphoma diagnosis since 01.01.2010 * Adult patients ≥ 18 years * Written informed consent Exclusion Criteria: * HIV-diagnosis \> 3 months after the diagnosis of malignant lymphoma * Non-Compliance or lack of opportunity for follow-up (for the prospective part of the study)

Where Is This Study? (1 UK site)

University Hospital of Wales

Cardiff, United Kingdom

NOT_YET_RECRUITING
Site contact (verified)

How to Get in Touch

Marcus Hentrich, MD

Sponsor contact

CONTACT

+49 89 1303 4372 marcus.hentrich@swmbrk.de

Kai Hübel, MD

Sponsor contact

CONTACT

+49 221 478 86177 kai.huebel@uk-koeln.de
Data sourced from ClinicalTrials.gov · Last verified: 2023-04