Collection of Blood Samples from a Population at Low Risk for HIV Infection
Tab Title Description
Describes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
- Rochester, Minnesota: 16-007864
Sponsor Protocol Number: COL-HIV- 403
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.
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.
Research participants from populations with less than 1% HIV prevalence.
Research participant ³18 years of age at time of collection.
Research participant has read, understood, signed, and dated the informed consent form, for California only, the Patient Bill of Rights form
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
Mayo Clinic principal investigator
Joseph Yao, M.D.
Closed for enrollment
Publications are currently not available