Actively Recruiting

Age: 18Years +
FEMALE
ID05566106

Anal Follow-up for Women With High-grade HPV-induced Gynecological Lesions

Led by Fondation Hôpital Saint-Joseph · Updated on 2022-10-06

1500

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Human Papillomavirus (HPV) infection is the most common sexually transmitted infection worldwide and is linked to approximately 4.5% of all cancers, including most cervical, vaginal, and anal cancers. Women with a history of high-grade HPV-induced gynecological lesions may have an increased risk of developing anal cancer. This research aims to study proctological follow-up for women at risk, based on age, smear results, and HPV tests, to better understand and manage the development of HPV-related anal lesions. This observational study proposes a proctology follow-up protocol for women considered at risk due to their history of high-grade HPV-induced gynecological lesions. The follow-up frequency is tailored according to the patient's age and risk factors, occurring every 3 years, 5 years, or annually. The study will observe patients participating in this follow-up to gather data on the risk of developing HPV-induced lesions and to develop a screening and anal follow-up model. Participants will undergo regular proctological examinations and follow-ups as part of the protocol. Researchers will monitor the risk of developing HPV-related lesions over time and assess the effectiveness of the proposed screening model. The study will measure outcomes during the first year and includes ongoing surveillance to improve clinical recommendations. Participants' data and health will be observed without intervention, with the study extending until the end of 2032.

CONDITIONS

Brief Title

Anal Follow-up of Patients With a Gynecological History of High-grade Lesion and More Induced HPV

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient aged 18 years or older
  • History of high-grade or higher HPV-induced gynecological lesion
  • Participating in the proctology follow-up protocol
  • French-speaking patient
Not Eligible

You will not qualify if you...

  • History of high-grade anal HPV lesion or higher
  • Under guardianship or curatorship
  • Deprived of liberty
  • Under court protection
  • Objecting to the use of personal data for this research

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - Up to 10 years

Participants with a history of high-grade HPV-induced gynecological lesions are observed for the risk of developing anal HPV-induced lesions.

1 to 2 visits per year depending on clinical follow-up

Trial Site Locations

Total: 1 location

1

Groupe Hospitalier Paris Saint-Joseph

Paris, France, 75014

Actively Recruiting

Loading map...

Research Team

S

Sophie Wylomanski, MD

H

Helene BEAUSSIER, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Similar Trials

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial