Feasibility of a Multi-site Screening Strategy in HPV+ Patients at High Risk of Cancer, With Characterization of the HPV Subtypes Involved by High Throughput Sequencing Technique: DEP-HPV

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The main risk of developing cervical cancer is the persistence of an High risk human papillomavirus (HPV-HR) infection, the mechanisms of which are still not understood. These chronically infected patients could develop multi-site lesions. The main objective is to assess the feasibility of setting up a personalized screening in patients at high risk of cervical cancer (chronically infected with HPV), by evaluating documenting the acceptability of these patients to be sampled from the ENT sphere and anal spheres for HPV analysis with next-generation sequencing.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Chronic infected patients defined by: Patients with persistent HPV-HR cytological infection (high risk) (as early as 6 months post-treatment of a cervical or vaginal injury), or a recurrence of a high-grade squamous intraepithelial lesion (CIN2 or CIN3 or HSIL) or a recurrence of cancer in the cervix or vagina

⁃ Patients who have given their written consent to participate in the study.

⁃ Person affiliated or beneficiary of a social security scheme.

Locations
Other Locations
France
CHU Toulouse
RECRUITING
Toulouse
Contact Information
Primary
Elodie Chantalat, MD
chantalat.e@chu-toulouse.fr
5.61.32.37.51
Time Frame
Start Date: 2022-06-21
Estimated Completion Date: 2025-12
Participants
Target number of participants: 30
Treatments
Experimental: Patients chronically infected with HPV
The study will be offered to patients with chronic HPV infection as part of an annual consultation scheduled in the gynecology care package.
Sponsors
Leads: University Hospital, Toulouse

This content was sourced from clinicaltrials.gov