RecruitingNot ApplicableNCT06522256

Identification of Molecular Signatures of High-risk Oncogenic HPV and Study of Their Associations With the Presence of High-grade Lesions and/or Anal Cancer 10 Years After Inclusion in the ANRS IPERGAY Trial


Sponsor

ANRS, Emerging Infectious Diseases

Enrollment

100 participants

Start Date

Mar 20, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

HPVsign is a cross-sectional, non-comparative, multicenter study involving all participants included in the HPV substudy of the ANRS IPERGAY trial. The study proposes to evaluate the cumulative incidence of high-grade lesions and/or anal cancers using high-resolution anoscopy (HRA) during the HPVsign study and/or diagnosed since the end of participation in the ANRS IPERGAY trial.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is a follow-up research project looking at people who participated in the ANRS IPERGAY clinical trial, specifically tracking whether certain high-risk strains of HPV (human papillomavirus) are linked to the development of high-grade anal lesions or anal cancer 10 years later. **You may be eligible if...** - You were a participant in the original ANRS IPERGAY trial and were enrolled in its HPV sub-study - You have signed informed consent - You are covered by a social security health insurance plan **You may NOT be eligible if...** - You are under legal guardianship or curatorship - You receive state medical assistance (free healthcare) - You disagree with the use of data collected during your participation in the IPERGAY trial Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREHigh-resolution anoscopy

The study includes 2 visits: * a medical consultation for inclusion * a proctology consultation including the performance of an AHR associated or not with biopsy sampling


Locations(3)

Hôpital de la Croix Rousse - SMIT

Lyon, France

Hôpital Saint-Louis - SMIT

Paris, France

Hôpital Tenon - SMIT

Paris, France

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NCT06522256


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