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OpenTrials
Completed

NCT Number: NCT00888771

Discard:Characterisation of Colonic Polyps in Vivo

Prospective study of accuracy of colonic polyp characterisation in vivo using high resolution white light endoscopy, narrow band imaging and chromoendoscopy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Wolfson Unit for Endoscopy, St Mark's Hospital

Harrow, Moddlesex, HA1 3UJ, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients over 18 years of age, assessed as fit for routine colonoscopy
  • Patients attending for screening or surveillance colonoscopy meeting the following criteria:
  • Polyp surveillance with at least 3 adenomas or 1 adenoma>10mm at previous colonoscopy
  • Surveillance post colorectal cancer resection
  • Screening with positive faecal occult blood test

Exclusion criteria

  • Patients with known colitis or polyposis syndromes
  • Unable or unwilling to give informed consent

Treatment and study plan

Primary outcomes

  1. Accuracy of polyp characterisation

    Time frame: 12 months

Secondary outcomes

  1. Change in surveillance interval after formal histopathology

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Imperial College London

Other

Registry information

Official study title

Characterisation of Small Colonic Polyps in Vivo

Acronym: DISCARD

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Apr 28, 2009
Registry last updated
Aug 5, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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