A meta-analysis of anal cancer incidence by risk group: Toward a unified anal cancer risk scale.
Gary M Clifford, Damien Georges, Meredith S Shiels...
https://pubmed.ncbi.nlm.nih.gov/32621759Actively Recruiting
Led by Fondation Hôpital Saint-Joseph · Updated on 2022-10-06
1500
Participants Needed
1
Research Sites
21 weeks
Total Duration
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
Anal Follow-up of Patients With a Gynecological History of High-grade Lesion and More Induced HPV
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
Total: 1 location
1
Groupe Hospitalier Paris Saint-Joseph
Paris, France, 75014
Actively Recruiting
S
Sophie Wylomanski, MD
H
Helene BEAUSSIER, MD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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