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Search / Trial NCT01882205

Comparison Between Chromoendoscopy and Virtual Chromoendoscopy (NBI, I-scan, FICE) for Detection of Neoplasia in Long Standing Ulcerative Colitis

Launched by UNIVERSITAIRE ZIEKENHUIZEN KU LEUVEN · Jun 17, 2013

Trial Information

Current as of September 01, 2025

Recruiting

Keywords

Ulcerative Colitis Dalm Chromoendoscopy Dysplasia Virtual Chromoendoscopy Fice Nbi I Scan

ClinConnect Summary

This clinical trial is comparing two different methods for checking for cancer in patients who have had ulcerative colitis for a long time. Ulcerative colitis is a condition that can increase the risk of colon cancer, especially after eight years from when it was first diagnosed. Currently, doctors follow guidelines that recommend taking many tissue samples during exams to look for cancer signs. However, this study aims to see if newer imaging techniques, like Narrow-Band Imaging (NBI) and Fujinon Intelligent Chromo-Endoscopy (FICE), are just as effective as the traditional method called chromo-endoscopy, but potentially easier and quicker.

To participate in this trial, individuals must have had ulcerative colitis for at least eight years, have had a previous endoscopy in the last year, and be able to give their consent. Unfortunately, people with active ulcerative colitis, a history of colon cancer, or those who are pregnant cannot take part. If eligible, participants can expect to undergo an endoscopic examination where doctors will use different imaging techniques to look for any signs of cancer, helping to improve future cancer screening methods for those with this condition.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients with longstanding ulcerative colitis ( 8 years after diagnosis or pancolitis and 10 years after diagnosis of left-sided colitis)
  • Signed informed consent form
  • Previous surveillance endoscopy \> 1 year
  • Exclusion Criteria:
  • Active ulcerative colitis, \> 20 cm from the margo ani
  • Personal history of colorectal cancer
  • Allergy or intolerance to methylene blue
  • Refusing or incapable to agree with informed consent
  • Age younger than 18 years
  • Pregnant women

About Universitaire Ziekenhuizen Ku Leuven

Universitaire Ziekenhuizen KU Leuven is a leading academic medical center in Belgium, renowned for its commitment to advancing healthcare through innovative research and clinical excellence. Affiliated with KU Leuven, one of Europe’s premier universities, the institution integrates cutting-edge scientific inquiry with high-quality patient care. It plays a pivotal role in the development and implementation of clinical trials, fostering collaboration between researchers, healthcare professionals, and industry partners to translate scientific discoveries into effective treatments. The hospital's multidisciplinary approach ensures comprehensive patient safety and ethical standards, positioning it as a trusted sponsor in the realm of clinical research.

Locations

Leuven, , Belgium

Roeselaere, , Belgium

Montreal, , Canada

Copenhagen, , Denmark

Maastricht, , Netherlands

Patients applied

0 patients applied

Trial Officials

Raf Bisschops, MD PhD

Principal Investigator

Universitaire Ziekenhuizen KU Leuven

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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