46
Participants
Start Date
June 30, 2011
Primary Completion Date
January 31, 2014
Study Completion Date
December 31, 2015
Venous blood samples, anal swab samples, vaginal swab samples, high resolution anoscopy (HRA), anal biopsy samples
"Before and at least 6 months after starting a new non-steroid immunosuppressive agent for IBD treatment, eligible participants who are attending for routine colonoscopy will have:~1. Anal swab samples (and vaginal swab samples for female participants) for human papillomavirus PCR typing (6, 11, 16, 18, 31, 33, 45, 52, 58)~2. High-resolution anoscopy and biopsy of all visible high-grade dysplastic lesions based on validated colposcopic criteria~3. Anal cytology testing"
University of Pittsburgh, Pittsburgh
Merck Sharp & Dohme LLC
INDUSTRY
University of Pittsburgh
OTHER