HPV DNA Clinical Trial
Official title:
Prevalence of Anal Dysplasia in Patients With Inflammatory Bowel Disease and Healthy Controls
This study is designed to establish the prevalence of anal squamous intraepithelial lesion (ASIL) in patients with inflammatory bowel disease (IBD) and healthy controls.
IBD patients attending the Stanford Inflammatory Bowel Disease (IBD) clinic and age-matched
healthy controls are screened for eligibility. Informed consent is obtained for eligible
subjects. An anonymous self-administered questionnaire is administered to assess risk
factors for HPV. For IBD patients, information regarding IBD diagnosis and treatment is
obtained.
An anal pap smear is performed at the time of a clinic visit or at the time of an already
scheduled colonoscopy. Samples are collected and processed at Stanford pathology where a
blinded pathologist reads all specimens. Human Papillomavirus (HPV) DNA testing is performed
on all specimens. All patients with anal squamous intraepithelial lesion (ASIL) are referred
to a colorectal surgeon for further recommendations or treatment, which includes a
high-resolution anoscopy.
;
Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Screening
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT04520464 -
Clinical Trial Comparing the Self-test for Cervicovaginal Sample Versus Samples From Service Provider (Xyto-Ro)
|
N/A |