Use of Accessory Device AmplifEYE During Average Risk Screening Colonoscopy to Increase Adenoma Detection Rate
| Status: | Recruiting |
|---|---|
| Conditions: | Colorectal Cancer, Gastrointestinal |
| Therapuetic Areas: | Gastroenterology, Oncology |
| Healthy: | No |
| Age Range: | 50 - 80 |
| Updated: | 8/24/2017 |
| Start Date: | August 3, 2017 |
| End Date: | March 2022 |
| Contact: | Alexander Jahng, MD |
| Email: | ajahng@llu.edu |
| Phone: | (909) 558-4905 |
The purpose of this investigator-initiated study is to determine whether the use of an
accessory device called AmplifEYE can improve colonoscopy quality in patients who are
undergoing average risk colorectal cancer screening. Primary end point is adenoma detection
rates.
accessory device called AmplifEYE can improve colonoscopy quality in patients who are
undergoing average risk colorectal cancer screening. Primary end point is adenoma detection
rates.
Inclusion Criteria:
- All adult patients greater than or at 50 years of age who are referred for average
risk screening colonoscopy.
Exclusion Criteria:
- Any pregnant patient
- Patient's that are unable to provide consent for themselves
- Any patient undergoing diagnostic colonoscopy (IBD, rectal bleeding, recent change in
bowel habits, etc.)
- Any patient undergoing surveillance (prior history of polyps or colorectal cancer)
- Any patient undergoing high risk screening colonoscopy (family history of colon cancer
in first degree family member <65 years of age, or co-existing conditions that
pre-dispose to colon cancer such as polyposis syndromes, PSC or IBD)
- Prior history of any cancer
- Current or past immunosuppression (due to either infection or medications)
- Coagulation disorder OR use of anti-coagulation or anti-platelet therapy other than
aspirin within 5-7 days of procedure
- Colonic strictures
- suspected intestinal obstruction or colonic pseudo-obstruction
- history of colon resection
- active infection
- active inflammation (including diverticulitis)
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