A multicenter prospective randomized controlled trial evaluating the usefulness of a real-time colonoscopy diagnostic support system
Not Applicable
Not yet recruiting
- Conditions
- Colorectal Neoplasms
- Registration Number
- JPRN-UMIN000051437
- Lead Sponsor
- Toho University Oomori hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 620
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients who underwent total colonoscopy within 2 years (24 months) 2) Patients with prior colectomy other than appendectomy 3) GI polyposis 4) Patients with complications, such as chronical hematological disease 5) Patients with active inflammatory bowel diseases, such as ulcerative colitis or Crohn's disease 6) pregnant patient
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Adenoma Detection Rate
- Secondary Outcome Measures
Name Time Method 1 ) Polyp Detection Rate 2 ) Adenoma per Positive Colonoscopy 3 ) Rate of increase in ADR by colonoscopy experience 4 ) Detection rate by lesion (size (6 mm or more, less than 6 mm), macroscopic type, location) 5 ) Sessile Serrated Lesion detection rate 6 ) Total procedure time