Self-sampling to Optimize Anal Lesion Outcomes

Recruiting N/A Interventional Study
Anal Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
35 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
572 (estimated)
Sponsor
Medical College of Wisconsin · Other
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About This Trial
The purpose of this research study is to find ways to increase anal cancer screening among people at increased risk for anal cancer. This study will try to find out if persons will do an intervention (self-sampling of the anal canal) and if it affects cytology and high-resolution anoscopy (HRA) appointment attendance. Secondarily, the study will assess if a person who gets their choice of either s…
Trial Locations
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Eligibility Criteria
A potential study subject who meets all of the following inclusion criteria is eligible to participate in the study. Note that these criteria apply regardless of HPV vaccination status or disability status. Inclusion Criteria: 1. Age ≥ 35 years for those who are HIV-positive or ≥ 45 years for thos…
Contacts

Alan G Nyitray, PhD

4149557701

anyitray@mcw.edu

CONTACT

Jenna Nitkowski, PhD

414-955-2126

jnitkowski@mcw.edu

CONTACT