AI boosts colonoscopy accuracy in massive new trial
NCT ID NCT07307547
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether an artificial intelligence (AI) system can help doctors spot more precancerous polyps and colorectal cancers during colonoscopy compared to standard procedures. Over 3,300 adults scheduled for screening or surveillance will be randomly assigned to AI-assisted or regular colonoscopy. The goal is to see if AI improves detection rates and reduces missed lesions, which could lead to earlier diagnosis and better outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 3,342 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age between 18 and 75 years, inclusive. 2. Scheduled for a screening, diagnostic, or surveillance colonoscopy. 3. Able to understand the study protocol and provide written informed consent. Exclusion Criteria: 1. Known contraindications to colonoscopy or biopsy. 2. Personal history of colorectal cancer, inflammatory bowel disease (IBD), or previous colorectal surgery. 3. Known or suspected colorectal polyposis syndrome (e.g., Familial Adenomatous Polyposis - FAP). 4. Patients with active colorectal bleeding, bowel obstruction, or toxic megacolon. 5. Women who are pregnant, planning to become pregnant, or are breastfeeding. 6. Participation in another interventional clinical trial within the 30 days prior to enrollment. 7. Any other condition that, in the investigator's judgment, would make the participant unsuitable for the study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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The Second Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, Zhejiang, 310009, China
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