Frontier Science & Technology Research Foundation, Inc.
Botswana Harvard Health Partnership
Brigham and Women's Hospital
Beth Israel Deaconess Medical Center
H. Lee Moffitt Cancer Center and Research Institute
University of North Carolina, Chapel Hill
National Cancer Institute (NCI)
Age
25–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
HIV-1 infection, as documented by:
1. any FDA-approved, licensed HIV rapid test performed in conjunction with screening (oral immunoblot, ELISA test kit, and confirmed by Western blot or other approved test), OR
2. a physician's written record that documents HIV infection with supporting information on the participant's relevant medical history and/or current management of HIV infection, OR
3. documentation of a prescription of an approved antiretroviral regimen by either possession of pill bottles or packages with prescriber's name or ARVs dispensed from an HIV clinical treatment program with participant identifiers affixed to the bottles or packages.
Aged 25 or older.
Ability to understand and the willingness to sign a written informed consent document by the participant or by the legal representative(s) of the participant.
Have an intact cervix.
You may not be if
Current symptoms or concern for cervical cancer.
History of cervical, vulvar, vaginal, perianal, anal cancer or oral cancer or current symptoms of cervical, vulvar, vaginal, perianal, anal cancer or oral cancer.
Have undergone cervical hHSIL treatment in the past year.
Have a history of hysterectomy with removal of the cervix.
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection (including opportunistic infections of AIDS and/or genitourinary infections), symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
Any other medical condition or social situation that would put the participant, the study staff, or the study outcomes at risk, as determined by the site investigators.
