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Utility of Random Biopsies in Patients With Inflammatory Bowel Disease (URBI)

Abramson Cancer Center at Penn Medicine logo

Abramson Cancer Center at Penn Medicine

Status

Invitation-only

Conditions

Ulcerative Colitis
Inflammatory Bowel Diseases
Crohn Disease

Treatments

Other: Biopsy strategy

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06560021
U01DK138901 (U.S. NIH Grant/Contract)
15225

Details and patient eligibility

About

The proposed study is a multicenter parallel group clinical trial that will include 821 evaluable patients per group who will be randomly assigned to either high definition white light colonoscopy (HDWLC) with targeted biopsies plus 2 random biopsies in 4 segments to assess for inflammation (limited biopsy strategy) or HDWLC with targeted biopsies plus 4 biopsies every 10 cm throughout the colon, at a minimum in all segments of the colon known to have been affected by IBD at any time, regardless of the extent of disease (random biopsy strategy). Participants will be followed until total proctocolectomy or the end of the study period to determine whether the two methods of surveillance colonoscopy are associated with detection of dysplasia or sessile serrated adenoma at follow-up colonoscopy. Follow-up via chart review may continue for up to 15 years from enrollment.

Full description

To maximize the yield of surveillance colonoscopy, minimize risk to patients, and deliver cost-effective care, it is imperative to resolve whether random biopsies are warranted for patients with long standing Inflammatory Bowel Disease (IBD) undergoing dysplasia and colorectal cancer (CRC) surveillance with high-definition white light colonoscopy (HDWLC). For this protocol, dysplasia surveillance refers to the process of identifying precancerous dysplasia, sessile serrated adenoma (SSA) or CRC. This protocol describes a pragmatic, multicenter randomized trial of patients with IBD undergoing dysplasia surveillance with HDWLC, the most common type of surveillance colonoscopy performed in the US, to definitively answer this question.

The primary objective of the study is to determine if HDWLC using a limited biopsy strategy is non-inferior to HDWLC using a random biopsy strategy to detect dysplasia or sessile serrated adenoma (SSA) in patients with IBD.

Secondary objectives include:

  1. Determine if HDWLC using a limited biopsy strategy is superior to HDWLC with a random biopsy strategy to detect one or more dysplastic or SSA lesion in patients with IBD
  2. Determine whether the number of targeted biopsies differs based on the number of random biopsies obtained.

Enrollment

1,642 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of left-sided (greater than 15 cm of disease but not beyond the splenic flexure) or extensive (extending beyond the splenic flexure) ulcerative colitis or IBD-U or colonic Crohn's disease involving at least 1/3 of the colon for at least 8 years
  • Patients who are scheduled to undergo colonoscopy as part of routine care.
  • At least one indication for the index colonoscopy must be to perform dysplasia surveillance.
  • Has not had a colonoscopy in the last 11 months

Exclusion criteria

  • Any condition that the endoscopist feels is a contraindication to random biopsies
  • History of visible (high or low grade) dysplasia not completely removed
  • History of sessile serrated adenoma not completely removed
  • History of colorectal cancer
  • Any condition for which the endoscopist feels that pancolonic contrast or virtual chromoendoscopy is mandatory
  • Inability to provide informed consent

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,642 participants in 2 patient groups

Limited biopsy strategy
Active Comparator group
Description:
Targeted biopsies plus 2 random biopsies in 2 segments to assess for inflammation
Treatment:
Other: Biopsy strategy
Random biopsy strategy
Active Comparator group
Description:
Targeted biopsies plus 4 biopsies every 10 cm throughout the colon, at a minimum in all segments of the colon known to have been affected by IBD at any time
Treatment:
Other: Biopsy strategy

Trial contacts and locations

17

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Central trial contact

Lisa C Nessel, MSS, MLSP; Brittaney Bonhomme, BS

Data sourced from clinicaltrials.gov

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