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Clinical Trial Summary

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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06296602
Study type Interventional
Source Centre Hospitalier Universitaire de Besancon
Contact Cedric LEBRETON, Dr
Phone 03 81 21 88 98
Email c1lebreton@chu-besancon.fr
Status Recruiting
Phase N/A
Start date March 4, 2024
Completion date November 4, 2024

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