Anal Human Papillomavirus in Inflammatory Bowel Disease Study

CompletedOBSERVATIONAL
Enrollment

46

Participants

Timeline

Start Date

June 30, 2011

Primary Completion Date

January 31, 2014

Study Completion Date

December 31, 2015

Conditions
Inflammatory Bowel Disease (IBD)Ulcerative Colitis (UC)Crohn's Disease (CD)Anal Human Papillomavirus
Interventions
PROCEDURE

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"

Trial Locations (1)

15213

University of Pittsburgh, Pittsburgh

All Listed Sponsors
collaborator

Merck Sharp & Dohme LLC

INDUSTRY

lead

University of Pittsburgh

OTHER

NCT01364896 - Anal Human Papillomavirus in Inflammatory Bowel Disease Study | Biotech Hunter | Biotech Hunter