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Clinical Trials in Taiwan / NCT07076966
Recruiting Not applicable

Comparison of Adenoma Detection Rate in 3D vs. 2D Surveillance Colonoscopy

NCT07076966 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2024-01-01
Last updated
2025-07-24

Condition(s) studied

ColonoscopyAdenoma Detection RateThree DimensionalColon Polyps and Adenomas

Investigational drug(s) / intervention(s)

3D device

3D device: Use 3D machine to generate the 3D image

Study summary

There is substantial evidence confirming that identifying and removing colorectal adenomas during colonoscopy helps prevent the development of colorectal cancer. Among the quality indicators for colonoscopy, adenoma detection rate (ADR) is the most important, as it is closely related to the patient's future risk of colorectal cancer. Recent studies have further demonstrated that improving ADR can reduce future mortality from colorectal cancer. Notably, non-polypoid lesions (such as flat or depressed lesions) are more likely to be missed during traditional colonoscopy, making these lesions a leading cause of post-colonoscopy interval colorectal cancer.

In a prospective trial conducted by our team comparing the ADR of 3D colonoscopy with standard 2D colonoscopy, we found that 3D colonoscopy significantly improved overall ADR and the detection rate of non-polypoid adenomas.

According to current international guidelines, after an index colonoscopy, patients are recommended to undergo surveillance colonoscopy 1 to 10 years later, depending on their findings at index colonoscopy. Since these patients represent the majority in clinical practice, increasing the ADR during surveillance colonoscopy not only allows for more precise recommendations for the timing of the next colonoscopy but also effectively reduces the risk of post-colonoscopy colorectal cancer (PCCRC).

Therefore, this multicenter, prospective, randomized trial aims to compare the clinical performance of 3D colonoscopy and standard 2D colonoscopy in the context of surveillance colonoscopy.

Eligibility

Sex
ALL
Min age
40 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Subjects who are 40 years of older * Subjects who receive colonoscopy and polypectomy more the 1 year * Subjects who need surveillance colonoscopy Exclusion Criteria: * Contraindication for colonoscopy * Subjects with familiar or hereditary polyposis * Subjects with history of colectomy * Inadequate bowel cleansing level * Subjects with inflammatory bowel disease

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
National Taiwan University Hospital, Hsinchu Branch Hsinchu Taiwan Recruiting
National Taiwan University Cancer Center Taipei Taiwan Recruiting
National Taiwan University Hospital Taipei Taiwan Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07076966 on ClinicalTrials.gov ↗ ← All trials in Taiwan