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Comparative study on the detectability of colonic adenomas in LCI and WLI in lower gastrointestinal endoscopy

Evaluation of availability of linked color imaging compared to white light imaging colonoscopy for detection of colonic adenomas: a multicenter prospective study - LCI-detection study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs072180006
Enrollment
600
Registered
2018-11-12
Start date
2018-12-03
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

lower gastrointestinal endoscopy examinee

Interventions

Subjects are randomized to the following two groups. group A: inspect at the first pass by LCI and the second pass by WLI group B: inspect at the first pass by WLI and the second pass by LCI

Sponsors

Shimoda Ryo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Lower GI endoscopy examinee who are between 18 and 79 years (at the time signing informed consent) 2) Patients who understand the contents of informed consent form and who can voluntarily sign informed consent form (in the case of a minor, also informed consent from proxies) 3) Patients who does not receive lower digestive tract endoscopy in the institute concerned for the past three years 4) Patients requiring lower digestive tract endoscopy (meeting any of the following criteria) (a)Positive fecal occult blood (b)Subjects with diagnosis or treatment history of large intestine adenoma, colorectal cancer (it is ineligible if colon/rectum resection was undertaken) (c)Subjects with digestive symptoms such as abdominal pain, diarrhea and constipation (d)Subjects who requires the screening of gastrointestinal cancer (e)Subjects with a family affection history of colorectal cancer and large intestine adenoma (f)Any other subjects who are regarded that the investigator needed lower digestive tract endoscopy

Exclusion criteria

Exclusion criteria: 1)Patients who have undergone intestinal resection 2)Patients with a history of inflammatory bowel disease 3)Patients with a history of familial adenomatous polyposis 4)Patients with a history of hereditary nonpolyposis colorectal cancer 5)Patients with severe intestinal adhesions known beforehand 6)Patients who the investigator determined difficult to participate in the study

Design outcomes

Primary

MeasureTime frame
miss rate

Secondary

MeasureTime frame
adenoma detection rate, number of adenomas detected at the first pass, miss subject rate, number of adenomas newly detected at second pass, proportion of total number of missed adenomas to total number of adenomas

Contacts

Public ContactRyo Shimoda

Saga University Hospital

shimoda1177@gmail.com+81-952-34-2361

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026