Consent for Use of Stored Patient Specimens for Future Testing
What You Need to Know Before You Apply
What is the purpose of this trial?
The purpose of this study is to obtain informed consent to use stored human biological materials (HBM) (e.g., blood and other tissues) for future studies that may include genetic testing.
Who Is on the Research Team?
David W. Haas, MD
Principal Investigator
Vanderbilt University Medical Center
Are You a Good Fit for This Trial?
Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Consent
Participants are asked to sign the informed consent form to allow their leftover samples to be used for secondary analyses and to have a blood sample drawn for DNA archiving
Sample Collection
Collection of 14 ml blood sample for DNA archiving for use in currently unspecified genetic analyses
Follow-up
Participants are monitored for any extraordinary circumstances that may require notification of test results from secondary testing
What Are the Treatments Tested in This Trial?
Interventions
- Consent for Use of Stored Patient Specimens for Future Testing
Find a Clinic Near You
Who Is Running the Clinical Trial?
Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
Lead Sponsor
AIDS Clinical Trials Group
Lead Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborator