Collection of Blood Samples from a Population at Low Risk for HIV Infection


About this study

The objective of this protocol is to collect EDTA-plasma and serum samples from adult subjects at low-risk for HIV infection. These samples will be used in Roche-sponsored clinical trial studies designed to evaluate molecular and serologic assays for the diagnosis and monitoring of HIV infection.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.


Inclusion Criteria

  1. Research participants from populations with less than 1% HIV prevalence.

  2. Research participant ³18 years of age at time of collection.

  3. Research participant has read, understood, signed, and dated the informed consent form, for California only, the Patient Bill of Rights form

Exclusion Criteria

       1. Known HIV positive

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Joseph Yao, M.D.

Closed for enrollment

More information


Publications are currently not available

Additional contact information

Non-cancer trials contact form

Phone: 800-664-4542 (toll-free)

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