A Registry Study on HIV-related Lymphoma

  • End date
    Aug 31, 2029
  • participants needed
  • sponsor
    Rotkreuzklinikum München gGmbH
Updated on 22 March 2022


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.


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.

Condition AIDS Related Lymphoma, HIV Related Lymphoma
Clinical Study IdentifierNCT05231135
SponsorRotkreuzklinikum München gGmbH
Last Modified on22 March 2022


Yes No Not Sure

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)
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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