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Completed

NCT Number: NCT04589078

Polyp REcognition Assisted by a Device Interactive Characterization Tool - The PREDICT Study

Diminutive colorectal polyps (≤ 5 mm) represent most of the polyps detected during colonoscopy, especially in the rectum-sigmoid tract. The characterization of these polyps by virtual chromoendoscopy is recognized as a key element for innovative imaging techniques. As a matter of facts diminutive colorectal polyps are very frequent and, if located in the rectosigmoid colon, they present a very low malignant risk (0.3% of evolution towards advanced adenoma and up to 0.08% of evolution towards invasive carcinoma). The real-time characterization would allow to identify the lowest risk polyps (hyperplastic subtype), to leave them in situ or, if resected, not to send them for histological examination, allowing a huge saving in healthcare associated costs.

Recently, the American Society for Gastrointestinal Endoscopy (ASGE) Technology Committee established the Preservation and Incorporation of Valuable endoscopic Innovations (PIVI) document, specific for real-time histological assessment for tiny colorectal polyps, to establish reference quality thresholds. Two performance standards have been developed to guide the use of advanced imaging:

1. for diminutive polyps to be resected and discarded without pathologic assessment, endoscopic technology (when used with high confidence) used to determine histology of polyps ≤ 5mm in size, when combined with the histopathology assessment of polyps > 5 mm in size, should provide a ≥ 90% agreement in assignment of post-polypectomy surveillance intervals when compared to decisions based on pathology assessment of all identified polyps; 2. in order for a technology to be used to guide the decision to leave suspected rectosigmoid hyperplastic polyps ≤ 5 mm in size in place (without resection), the technology should provide ≥ 90% negative predictive value (when used with high confidence) for adenomatous histology.

Computer-Aided-Diagnosis (CAD) is an artificial intelligence-based tool that would allow rapid and objective characterization of these lesions. The GI Genius CADx was developed to help endoscopists in their clinical practices for polyps characterization.

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Key information

Age range

40 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Endoscopy Unit, Humanitas Research Hospital

Rozzano, Milano, 20089, Italy

Who can participate

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

Inclusion criteria

  • Patients aged 40-80 undergoing screening colonoscopy for CRC
  • Ability to provide written, informed consent (approved by EC) and understand the responsibilities of trial participation.

Exclusion criteria

  • subjects positive to Fecal Immunochemical Test or Fecal Occult Blood Test;
  • subjects undergoing CRC surveillance colonoscopy
  • subject at high risk for CRC
  • subjects with a personal history of CRC, IBD or hereditary polyposic or non-polyposic syndromes;
  • patients with previous resection of the sigmoid rectum;
  • patients on anticoagulant therapy, which precludes resection / removal operations due to histopathological findings;
  • patients who perform an emergency colonoscopy.

Treatment and study plan

GI Genius CADe system

Device

Each patient will undergo standard white-light colonoscopy with the support of the latest version of the CE marked GI Genius CADe available.

Primary outcomes

  1. Negative Predictive Value of histology prediction on diminutive (≤5 mm) rectosigmoid polyps

    Time frame: 1 day

Secondary outcomes

  1. Agreement in assignment of post-polypectomy surveillance intervals

    Time frame: 1 day

    Agreement in assignment of post-polypectomy surveillance intervals according to established guidelines between:

    • the assignment identified according to the combined
    • GI Genius CADx histology prediction for diminutive (≤5 mm) polyps and
    • histology for larger polyps (> 5 mm), and
    • the assignment identified according to histology only.

Other outcomes

  1. Sensitivity, Specificity, Accuracy, PPV and NPV of GI Genius CADx histology prediction and endoscopist assessment on all the identified lesions

    Time frame: 1 day

Sponsors and collaborators

Lead sponsor

Cosmo Artificial Intelligence-AI Ltd

Industry

Registry information

Acronym: PREDICT

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Oct 19, 2020
Registry last updated
May 12, 2021

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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