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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03361917
Other study ID # 1709336500
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 11, 2017
Est. completion date April 18, 2018

Study information

Verified date July 2019
Source Indiana University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study seeks to compare colonoscopy results between a standard method and one using a distal scope attachment (Endocuff Vision).


Description:

For this study, subjects will be randomized into one of two groups (those who receive a standard colonoscopy and those who receive a colonoscopy with an Endocuff Vision attachment). Results will then be compared between the two; these include insertion time (time it takes to reach the cecum of the large intestine), inspection time (time spent examining the large intestine), the total time per each polypectomy (removal of polyps in the colon), and the total procedure time of the colonoscopy.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date April 18, 2018
Est. primary completion date April 18, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Subject referred for a screening or surveillance colonoscopy

- Subject is aged 40 years or older

- Subject has the ability to provide informed consent

Exclusion Criteria:

- Prior history of colon cancer

- History of inflammatory bowel disease

- Prior surgical resection of any part of the colon

- Use of antiplatelet agents or anticoagulants that precludes the removal of polyps during the procedure

- History of polyposis syndrome or HNPCC

- Family history of colon cancer in a first-degree relative < 60 years or two first degree relatives with colorectal cancer

- Inability to provide informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Endocuff Vision
Subjects that are randomized to undergo their colonoscopy procedure with the Endocuff Vision device will have the device placed on the colonoscope that will be used during their procedure.

Locations

Country Name City State
United States Indiana University Indianapolis Indiana

Sponsors (1)

Lead Sponsor Collaborator
Indiana University

Country where clinical trial is conducted

United States, 

References & Publications (1)

Tsiamoulos ZP, Misra R, Rameshshanker R, Elliott TR, Beintaris I, Thomas-Gibson S, Haycock A, Suzuki N, Rees C, Saunders BP. Impact of a new distal attachment on colonoscopy performance in an academic screening center. Gastrointest Endosc. 2018 Jan;87(1):280-287. doi: 10.1016/j.gie.2017.04.001. Epub 2017 Apr 13. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Inspection Time Comparisons for Each Method (Standard vs. Endocuff Vision) Inspection time is time spent actually examining the colon. This was measured with a stopwatch and calculated by subtracting washing, suctioning, polypectomy and biopsy times from total withdrawal time. It was measured during colonoscopy by a study assistant using a stopwatch. During the withdrawal portion of the colonoscopy procedure
Secondary Insertion Time Comparisons for Each Method (Standard vs. Endocuff Vision) Insertion time is the time it takes from the colonoscope first being inserted to when the furthest section of the colon (which is called the cecum) is reached. During the insertion portion of the colonoscopy procedure
Secondary Total Procedure Time Comparisons for Each Method (Standard vs. Endocuff Vision) Total procedure time is the time from the initial insertion through the complete withdrawal of the scope During the colonoscopy procedure
Secondary Detection Rates The percentage of participants with at least one of the indicated polyp types found during standard colonoscopy compared to colonoscopy with Endocuff Vision. During the colonoscopy procedure
Secondary Polyps Per Colonoscopy Number of adenomas or sessile serrated polyps found per colonoscopy of Standard colonoscopy compared to Colonoscopy with Endocuff Vision. During the colonoscopy procedure
Secondary Boston Bowel Preparation Score Boston Bowel Preparation Score for patients receiving standard colonoscopy compared to colonoscopy with endocuff vision.
The total score for the Boston Bowel Preparation Scale ranges from 0 to 9, with higher score indicating a better bowel preparation quality.
The quality of the bowel preparation is assessed by the attending gastroenterologist.
During the withdrawal portion of the colonoscopy procedure after cleaning of the colon
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