Clinical Trials Directory

Trials / Recruiting

RecruitingNCT03061435

Screening for Anal Cancer in Women With High-grade Vulvar Dysplasia or Vulvar Cancer.

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
110 (estimated)
Sponsor
Dr. Danielle Vicus · Academic / Other
Sex
Female
Age
40 Years
Healthy volunteers
Accepted

Summary

Almost half of all women will develop an HPV infection in their lifetime. While most infections are naturally asymptomatic or cleared by the immune system, some persist and can lead to the development of cervical, vulvar, or anal lesions and eventually cancer. Screening regimens for these lesions are currently only in place for the cervix through regular Pap tests. These Pap tests usually involve an examination of the vulva -however, no screening procedures exist for anal cancer for women. Several studies have suggested that women with existing gynecological lesions are more likely to develop anal lesions and anal cancer. Here the investigators propose a multi-center study which seeks to screen for and treat anal cancer in women over the age of 40 with vulvar lesions and a stable immune system. The investigators will achieve this through performing anal Pap smears on eligible women and conducting High Resolution Anoscopy (HRA) and appropriate treatment procedures on those with abnormal anal cells. With enough evidence, there may be an indication to establish regular anal cancer screening measures in this potentially underserved population. Hypothesis: The investigators hypothesize that at least 40% of women with vulvar cancer or VIN2/3 will have abnormal anal cytology. 35% of the population will be hrHPV DNA positive and 11% will additionally have AIN2/3. This prospective study may lay the groundwork for routine anal screening regimens in Ontario and help shift health policy to treat this population.

Conditions

Interventions

TypeNameDescription
PROCEDUREScreening anal Pap smear - No high-resolution anoscopy75% of patients with negative cytology on their anal Pap smear will not receive high-resolution anoscopy
PROCEDUREScreening anal Pap smear - High-resolution anoscopy25% of patients with negative cytology on their anal Pap smear will receive high-resolution anoscopy. All patients with positive (abnormal) cytology on their anal Pap smear will receive high-resolution anoscopy.

Timeline

Start date
2021-02-01
Primary completion
2025-08-01
Completion
2026-01-01
First posted
2017-02-23
Last updated
2025-05-16

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03061435. Inclusion in this directory is not an endorsement.