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Evaluation of colonoscopy insertion technique improvement in trainees from various countries using Mikoto colonoscopy model (International Mikoto Study)

Evaluation of colonoscopy insertion technique improvement in trainees from various countries using Mikoto colonoscopy model (International Mikoto Study) - International Mikoto Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060082
Enrollment
420
Registered
2025-12-15
Start date
2024-06-14
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

Colonoscopy recipients

Interventions

Sponsors

Saga University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients between 18 and 90 who undergo colonoscopy 2) Patients who need colonoscopy (patients who meet one of the following conditions) Patients with positive fecal immunochemical test Patients who have been diagnosed or treated for colorectal adenoma or colorectal cancer (patients who have undergone colorectal resection are not eligible) Patients with gastrointestinal symptoms such as abdominal pain, diarrhea, constipation, etc Patients who need to be screened for gastrointestinal cancer Patients with a family history of colorectal cancer or colorectal adenoma

Exclusion criteria

Exclusion criteria: 1) Patients who have undergone bowel 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 non-polyposis colorectal cancer 5) Patients with previously known severe intestinal adhesions 6) Patients with severe obesity (BMI > 35 kg/m2) 7) Patients who are pregnant 8) Patients whose previous colonoscopy was judged by the investigator to have been difficult to insert (insertion time > 15 minutes) or who had poor colonoscopy preparation (Modified Aronchick Scale: Poor/Inadequate) 9) Patients who are judged by the investigator to be unable to participate in the study. 10) Patients who declared non-participation in the study

Design outcomes

Primary

MeasureTime frame
cecal intubation rate

Countries

Japan,Asia(except Japan),North America

Contacts

Public ContactDaisuke Yamaguchi

Saga University Gastroenterology

daisukehawks@gmail.com0952316511

Outcome results

None listed

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