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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02552017
Other study ID # 039/2014
Secondary ID 177181182104
Status Recruiting
Phase N/A
First received September 10, 2015
Last updated September 15, 2015
Start date November 2014
Est. completion date June 2016

Study information

Verified date September 2015
Source South Tyneside NHS Foundation Trust
Contact Wee Sing Ngu, MBChB, MRCS
Phone 01914041000
Email wngu@nhs.net
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if a new device, called the Endocuff Vision (a small plastic device attached to the end of the colonoscope which helps by holding the folds of the bowel back to give a clear view of the inside of the bowel) will significantly improve the detection of adenomas when used in all patients referred for colonoscopy.


Description:

Bowel cancer is common in the United Kingdom, with around 1 in 16 men and 1 in 20 women developing it at some point in their lives. Most bowel cancers happen when a type of polyp (a growth in the bowel) called an adenoma becomes cancerous. Doctors use a camera test, known as a colonoscopy, to look inside the bowel and find these polyps and remove them. Removing precancerous polyps is known to reduce the chances of a person developing bowel cancer in the future. How good colonoscopists are at finding these polyps varies, and there is a lot of research into how to improve "adenoma detection rates".

A new device, called the Endocuff Vision (a small plastic device attached to the end of the colonoscope which helps by holding the folds of the bowel back to give a clear view of the inside of the bowel) has been shown to improve the rate of polyp detection at colonoscopy, and to make polyp removal easier. Previous small studies have shown that there is a significant improvement in detection of adenomas when an Endocuff Vision is used (with the rate of detection of adenomas rising from 49% to 66%). Colonoscopists who have used the Endocuff Vision before also feel that polyp removal is easier when it is on the colonoscope. This study will randomise patients coming for colonoscopy to have their procedure performed as usual (i.e. without the Endocuff Vision attached) or as an Endocuff Vision-assisted colonoscopy. The investigators will record polyp and adenoma detection rates, duration of procedure, participant comfort levels, and complications. All patients referred for colonoscopy (via the symptomatic service, surveillance procedures, and the Bowel Cancer Screening Programme) will be invited in 7 centres (a mixture of specialist centres and district general hospitals), recruiting a total of 1772 participants.


Recruitment information / eligibility

Status Recruiting
Enrollment 1772
Est. completion date June 2016
Est. primary completion date June 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. All patients referred for screening, surveillance, or diagnostic colonoscopy

2. All patients must be able to give informed consent

Exclusion Criteria:

1. Patients with any absolute contraindications to colonoscopy

2. Patients with established or suspicion of large bowel obstruction or pseudo-obstruction

3. Patients with known colon cancer or polyposis syndromes

4. Patients with known colonic strictures

5. Patients with known severe diverticular segments (that is likely to impede colonoscope passage)

6. Patients with active colitis (ulcerative colitis, Crohn's colitis, diverticulitis, infective colitis)

7. Patients lacking capacity to give informed consent

8. Pregnancy

9. Patients who are on clopidogrel, warfarin, or other new generation anticoagulants who have not stopped this for the procedure.

10. Patients who are attending for a therapeutic procedure or assessment of a known lesion

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Device:
Endocuff Vision
Endocuff Vision is a new device made of soft plastic material with a unique dynamic shape. It is manufactured by ARC Medical Design Limited and Diagmed in the United Kingdom. It has European Conformity in United Kingdom. The core is made of polypropylene and the 'finger like' projections are made of a thermoplastic elastomer. It comes in four colour coded sizes (purple, blue, green and orange) to fit a range of paediatric and adult colonoscopes. Endocuff Vision is the more updated version of device that has only one proximal row of more rounded finger-like projections. It is mounted at the tip of the colonoscope and held on by friction (pull-off force is a minimum of 10 Newtons).

Locations

Country Name City State
United Kingdom County Durham and Darlington NHS Foundation Trust Durham County Durham
United Kingdom St Mark's Hospital and Academic Institute Harrow Middlesex
United Kingdom South Tees Hospitals NHS Foundation Trust Middlesbrough North Yorkshire
United Kingdom Northumbria Healthcare NHS Foundation Trust North Shields Tyne and Wear
United Kingdom South Tyneside NHS Foundation Trust South Shields Tyne and Wear
United Kingdom North Tees and Hartlepool NHS Foundation Trust Stockton-on-Tees County Durham
United Kingdom City Hospitals Sunderland NHS Foundation Trust Sunderland Tyne and Wear

Sponsors (1)

Lead Sponsor Collaborator
South Tyneside NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adenoma detection rate A difference in adenoma detection rate between Endocuff Vision-assisted colonoscopy and standard colonoscopy. 10 months No
Secondary Mean adenomas detected per procedure A difference in mean adenomas detected per procedure between both groups 10 months No
Secondary Rate of cuff exchange The rate of cuff exchange (that is, how often the cuff has to be removed) between both groups 10 months No
Secondary Effect on duration of caecal intubation rates Duration of complete withdrawal time in procedures where no polyps are detected between both groups 10 months No
Secondary Patient satisfaction using validated patient comfort Bowel Cancer Screening Programme (BCSP) questionnaires Patient satisfaction measured from no pain (0) to severe pain (3), episodes of discomfort from no discomfort (0) to frequent (more than 4 times)(3), length of discomfort from no discomfort (0) to more than 1 minute(3). 10 months No
Secondary Increase in surveillance colonoscopies caused by increased adenoma detection rate Increase in surveillance colonoscopies due to increased adenoma detection rate in terms of number of potential follow up procedures based on British Society of Gastroenterology adenoma surveillance guidelines in both groups 10 months No
Secondary Number of proximal sessile serrated polyps by histology Number of of proximal sessile serrated polyps in both groups 10 months No
Secondary Polyp location Distribution of polyps in the colon in both groups by location 10 months No
Secondary Adenoma detection rate of BCSP and non-BCSP endoscopists Adenoma detection rate of BCSP and non-BCSP colonoscopists 10 months No
Secondary Change in adenoma detection rate of each endoscopist during the course of the trial Adenoma detection rate (ADR) of the first 20% of patients scoped by each colonoscopist with the last 20% of patients in each arm to identify any changes in ADR. 10 months No
Secondary Adenoma detection rate of individual endoscopist before and after trial commencement Baseline ADR of each colonoscopist prior to trial recruitment with their individual ADR in patients where Endocuff Vision was not used. 10 months No
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