Phase
Condition
N/ATreatment
None - observational study only
Clinical Study ID
Ages 18-40 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Female at birth
Willing and able to provide informed consent for screening and cognitive ability tounderstand sampling procedures
Not pregnant
HIV negative on testing performed by study staff
18-40 years old
Planning to stay in the area for the next 10 weeks
Able and willing to provide adequate locator information for study retentionpurposes
Willing and able to return for all 3 nurse visits and return self-swabs to theclinic weekly
Sexually active for the last 3 months defined as penetrative penile-vaginalintercourse at least once in the last 3 months
Exclusion
Exclusion Criteria:
Male at birth
Not willing to provide consent
Pregnant or actively trying to conceive/become pregnant in the next 10 weeks
Living with HIV or untreated STIs (CT, NG, TV) or bacterial vaginosis (Nugent > 3)
Currently taking antibiotics or having been on antibiotic treatment in the previousfour weeks
<18 or >40 years old
On chronic disease management for gynaecological conditions
Any medical condition or other factors which would preclude study participation asper principal Investigator's or designee's decision, including but not limited tocancer of the cervix
Any mental health condition which, in the opinion of the investigator, wouldpreclude comprehension of informed consent, or preclude study participation
Currently enrolled on any other study prohibiting co-enrolment
Study Design
Study Description
Connect with a study center
KEMRI
Kisumu, 40100
KenyaActive - Recruiting
Desmond Tutu Health Foundation
Cape Town, Western Cape 7975
South AfricaActive - Recruiting
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