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NCT06216405Completed

Performance of Artificial Intelligence in Colonoscopy for Right Colon Polyp Detection

Performance of Artificial Intelligence in Colonoscopy for Right Colon Polyp Detection: a Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 23 Jan 2024

Brief summary (registry, in English)

The aim of the study is to assess whether the use of artificial intelligence improves polyp detection in a segment of the colon (the right colon). To achieve this objective, patients will be divided into two groups: one will undergo a standard colonoscopy, the other a colonoscopy with the artificial intelligence software connected to the machine. This software does not modify the colonoscopy technique in any way, and does not require the administration of any product to the patient. The study will compare the detection rate of right colon polyps between the group of patients who underwent standard colonoscopy and those who underwent colonoscopy with artificial intelligence. If this number does not differ between the two groups, the investigators can conclude that there is no point in using artificial intelligence.

Status (registry)
Completed
Study type
Interventional
Enrollment
2000 (actual)
First submitted
11 Jan 2024
Start date
20 Jan 2022
Primary completion date
12 Dec 2023
Lead sponsor
Groupe Hospitalier Diaconesses Croix Saint-Simon
NCT number
NCT06216405

What you commit to

  • Study type: Interventional
  • Participants enrolled: 2000
  • From 20 Jan 2022 to the primary completion date, 12 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with history of inflammatory bowel diseases
  • Patients with history of familial polyposis syndrome
  • Patients with history of right colonic resection.
  • People under psychiatric care who are not able to understand the aim if this research

Other

  • Pregnant or breastfeeding women
  • Patient benefiting from a legal protection measure : tutorship, curatorship, patient deprived of freedom
  • Adults who are unable to give their consent

Who the study is looking for

  • Age\>18 years
  • Signed informed consent
  • Affiliated to or beneficiary of a social security scheme

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Groupe Hospitalier Diaconesses Croix Saint-Simon
Coordinator of this site? Confirm its status
ParisFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.