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Evolution of Cellular and Viral Resistance in HIV-infected Patients With Lymphoma
Conditions
HIV - Lymphoma
Conditions: official terms
Lymphoma
Study Type
Observational
Study Phase
N/A
Study Design
Observational Model: Case Control
Overall Status
Recruiting
Summary
The study's chief objective is to observe the evolution of cellular (in terms of expression of transmembrane transporters and their transcriptional regulators) and viral resistance (in terms of development of mutations in the HIV genome that may confer resistance to future treatment for HIV) in HIV-infected patients with lymphoma.
Detailed Description
The study team will take two or three tubes of blood on three occasions during the course of chemotherapy. The total amount of blood required for this research project is 64mL (approximately 4 tablespoons).
This will allow better understanding of the changes that take place in the blood and the HIV virus itself. It is hoped that this will provide new insights that may aid the understanding and treatment of HIV patients with lymphoma.
This will allow better understanding of the changes that take place in the blood and the HIV virus itself. It is hoped that this will provide new insights that may aid the understanding and treatment of HIV patients with lymphoma.
Criteria for eligibility
Healthy Volunteers: No
Maximum Age: N/A
Minimum Age: N/A
Gender: Both
Criteria: Inclusion Criteria:
- The ability to understand and sign a written informed consent form, prior to participation in any screening procedure and must be willing to comply with all study requirements.
- Documented HIV-1 infection.
- Diagnosis of lymphoma (with the exclusion of the five subjects that will be controls).
- On cART or about to start cART as part of clinical routine care before the initiation of chemotherapy.
Exclusion Criteria:
- Receiving anti-tuberculosis treatment.
- The ability to understand and sign a written informed consent form, prior to participation in any screening procedure and must be willing to comply with all study requirements.
- Documented HIV-1 infection.
- Diagnosis of lymphoma (with the exclusion of the five subjects that will be controls).
- On cART or about to start cART as part of clinical routine care before the initiation of chemotherapy.
Exclusion Criteria:
- Receiving anti-tuberculosis treatment.
Location
St Stephen's Centre
London, United Kingdom
Status: Recruiting
Contact: Marta Boffito, Dr - marta.boffito@chelwest.nhs.uk
Start Date
May 2011
Completion Date
May 2014
Sponsors
St Stephens Aids Trust
Source
St Stephens Aids Trust
Record processing date
ClinicalTrials.gov processed this data on July 28, 2015
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