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NCT00587912 Clinical Trial

AIDS and Cancer Specimen Bank (ACSB)

Cancer Clinical Trial

Official title:
AIDS and Cancer Specimen Bank (ACSB)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00587912
Other study ID # 97-043
Secondary ID
Status Completed
Phase N/A
First received December 24, 2007
Last updated April 20, 2011
Start date June 1997
Est. completion date April 2011

Study information
Verified date April 2011
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to obtain clinical specimens from pathologists and physicians involved in the diagnosis and care of patients with AIDS and non-AIDS associated malignancies.

The National Cancer Institute has set up a Bank for tissues and biological fluids from HIVpositive and HIV-negative individuals in order to have specimens available for scientists studying malignancies associated with HIV disease.

Description:

The overall goal of the AIDS and Cancer Specimen Bank is to obtain clinical specimens from pathologists and physicians involved in the diagnosis and care of patients with AIDS and non- AIDS associated malignancies. These specimens will be banked and linked to a clinical data set so that experimental results obtained by analysis of specific specimens can be linked to relevant clinical data. Contents of the ACSB will be made available to researchers through an application to the National Cancer Institute. Strict patient confidentiality protection guidelines are in place for all specimens in the ACSB. The objective of this protocol is to obtain clinical specimens from potential participants in clinical trials conducted by the AIDS Malignancies Consortium, and from other patients with and without HIV infection, who have AIDS-Associated malignancies.

Recruitment information / eligibility
Status Completed
Enrollment 65
Est. completion date April 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient > 18 years of age

- Suspected or confirmed AIDS-Associated malignancy with or without HIV infection

- Will obtain fresh tissue and/or biological fluids

- Patient signed the correct version of the informed consent

Exclusion Criteria:

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Memorial Sloan-Kettering Cancer Center New York New York

Sponsors (6)
Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center George Washington University, Kaiser Permanente, National Cancer Institute (NCI), University of California, San Francisco, University of Hawaii

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Identify and improve access to tumor tissue, biological specimens, and associated clinical outcome data that could be utilized for research by the research community at-large on the pathogenesis of HIV and non-HIV associated malignancies. 3 years No
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