Impact of a new detachable device ”New endoscopic cap”, on the improvement of colonoscopy quality

Impact of a new detachable device ”New endoscopic cap”, on the improvement of colonoscopy quality: a prospective randomized study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005214

Enrollment

528

Registered

2020-07-10

Start date

2020-07-13

Completion date

Unknown

Last updated

2021-12-02

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

Conditions

None listed

Interventions

Medical Device : After 1:1 randomization, we will perform colonoscopy divided into groups of new endoscopic cap and control groups.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Aged over 18 who have agreed to participate in this study

Exclusion criteria

Exclusion criteria: (1) A patient previously diagnosed with colorectal cancer or colorectal polyposis (2) A suspected colonic obstruction (3) A patient who has undergone a surgery related to the colon (4) A patient with inflammatory bowel diseases such as ulcerative colitis and Crohn's disease. (5) A patient unable to stop anticoagulant or anti-platelet agents (6) Pregnant and breastfeeding women (7) Patients who are unable to evaluate proper colonoscopy due to underlying disease

Design outcomes

Primary

Measure	Time frame
Independent cecal intubation rate and time;Adenoma detection rate	—

Secondary

Measure	Time frame
Total procedure time;Adenoma per colonoscopy;Polyp resection method and time;Adenoma detection rate by the site of polyp;Detection rate of sessile serrated polyp;Adenoma detection rate by the size of polyp;Cecal intubation rate and adenoma detection rate in accordance with the experience of colonoscopy	—

Countries

Korea, Republic of

Contacts

Public ContactSeung Wook Hong

Asan Medical Center

hswooki@gmail.com+82-2-3010-0160

Outcome results