Polyp Detection With the EndoRings™: A Randomized Tandem Colonoscopy Study
Completed · Not applicable
Conditions studied: Colon Cancer
In brief
To compare the adenoma miss rate with the EndoRings™ vs. the adenoma miss rate with Standard view colonoscopy. To compare the polyp miss rate with the EndoRings™ vs. the polyp miss rate with Standard view colonoscopy.In addition, time measurements including time to cecum, time for withdrawal and overall procedure time will be analyzed and reported for each group.
Key facts
- Study ID
- NCT01955122
- Run by
- EndoAid
- People needed
- 126
- Starts
- 2013-07-01
- Expected to finish
- 2014-07-01
- Last updated by the study team
- 2017-03-06
Who can join
Age: 40 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Subject between the ages of 40 and 75
- The patient is undergoing colonoscopy for screening, for surveillance in follow-up of previous polypectomy or for diagnostic workup;
- Written informed consent must be available before enrollment in the trial
You may not qualify if…
- Patients with a history of colonic resection;
- Patients with known (or newly diagnosed) inflammatory bowel disease;
- Patients with a personal history of polyposis syndrome;
- Patients with suspected chronic stricture potentially precluding complete colonoscopy;
- Patients with diverticulitis or toxic megacolon;
- Patients with a history of radiation therapy to abdomen or pelvis;
- Patients with a hemorrhagic diathesis
- Patients with acute lower GI bleeding
- Pregnant women and women with childbearing potential without adequate contraception
- Patients who are currently enrolled in another clinical investigation in which the intervention might compromise the safety of the patient's participation in this study.
Where it is running
- Indiana University — Indianapolis, Indiana, United States
- Elisha Medical Center — Haifa, Please Select, Israel
- University Medical Center Utrecht — Utrecht, Netherlands
Full record on ClinicalTrials.gov
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