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This is an interventional study investigating HPV carriage and liquid-based cytology at anal level. It will be offered to all patients undergoing PreP consultations at Besançon University Hospital. The anal swab will be taken by the doctor using a cyto-brush during the consultation.
Full description
The duration of participation in the study is 3 months for the submission of the results of the samples. A medical proctology consultation may also be offered, depending on the results of the screening.
This will be carried out in addition to the anal swabs taken quarterly to screen for other sexually transmitted infections.
A questionnaire will be completed by the doctor to record the data of interest. From additional data already entered in the e-NADIS software will be included for study.
Enrollment
Sex
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Volunteers
Inclusion criteria
Men sex Men Using Pre-exposure Prophylaxis for HIV Follow up au CHU de Besançon.
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
100 participants in 1 patient group
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Central trial contact
Cedric LEBRETON, Dr; Ingrid TISSOT
Data sourced from clinicaltrials.gov
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