Accuracy of Detection Using ENdocuff Optimisation of Mucosal Abnormalities (ADENOMA)
Primary Purpose
Colorectal Neoplasms, Colonic Polyps, Adenoma
Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Endocuff Vision
Sponsored by
About this trial
This is an interventional diagnostic trial for Colorectal Neoplasms focused on measuring adenoma detection rate, Endocuff, Endocuff Vision, colonoscopy, bowel cancer screening, bowel cancer
Eligibility Criteria
Inclusion Criteria:
- All patients referred for screening, surveillance, or diagnostic colonoscopy
- All patients must be able to give informed consent
Exclusion Criteria:
- Patients with any absolute contraindications to colonoscopy
- Patients with established or suspicion of large bowel obstruction or pseudo-obstruction
- Patients with known colon cancer or polyposis syndromes
- Patients with known colonic strictures
- Patients with known severe diverticular segments (that is likely to impede colonoscope passage)
- Patients with active colitis (ulcerative colitis, Crohn's colitis, diverticulitis, infective colitis)
- Patients lacking capacity to give informed consent
- Pregnancy
- Patients who are on clopidogrel, warfarin, or other new generation anticoagulants who have not stopped this for the procedure.
- Patients who are attending for a therapeutic procedure or assessment of a known lesion
Sites / Locations
- County Durham and Darlington NHS Foundation TrustRecruiting
- North Tees and Hartlepool NHS Foundation TrustRecruiting
- St Mark's Hospital and Academic InstituteRecruiting
- South Tees Hospitals NHS Foundation TrustRecruiting
- Northumbria Healthcare NHS Foundation TrustRecruiting
- South Tyneside NHS Foundation TrustRecruiting
- City Hospitals Sunderland NHS Foundation TrustRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Endocuff Vision-assisted Colonoscopy
Standard Colonoscopy
Arm Description
Participants in this arm undergo Endocuff Vision-assisted colonoscopy
Participants in this arm undergo standard colonoscopy
Outcomes
Primary Outcome Measures
Adenoma detection rate
A difference in adenoma detection rate between Endocuff Vision-assisted colonoscopy and standard colonoscopy.
Secondary Outcome Measures
Mean adenomas detected per procedure
A difference in mean adenomas detected per procedure between both groups
Rate of cuff exchange
The rate of cuff exchange (that is, how often the cuff has to be removed) between both groups
Effect on duration of caecal intubation rates
Duration of complete withdrawal time in procedures where no polyps are detected between both groups
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).
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
Number of proximal sessile serrated polyps by histology
Number of of proximal sessile serrated polyps in both groups
Polyp location
Distribution of polyps in the colon in both groups by location
Adenoma detection rate of BCSP and non-BCSP endoscopists
Adenoma detection rate of BCSP and non-BCSP colonoscopists
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.
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.
Full Information
NCT ID
NCT02552017
First Posted
September 10, 2015
Last Updated
September 15, 2015
Sponsor
South Tyneside and Sunderland NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT02552017
Brief Title
Accuracy of Detection Using ENdocuff Optimisation of Mucosal Abnormalities
Acronym
ADENOMA
Official Title
Accuracy of Detection Using ENdocuff Optimisation of Mucosal Abnormalities
Study Type
Interventional
2. Study Status
Record Verification Date
September 2015
Overall Recruitment Status
Unknown status
Study Start Date
November 2014 (undefined)
Primary Completion Date
June 2016 (Anticipated)
Study Completion Date
June 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
South Tyneside and Sunderland NHS Foundation Trust
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief 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.
Detailed 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Neoplasms, Colonic Polyps, Adenoma
Keywords
adenoma detection rate, Endocuff, Endocuff Vision, colonoscopy, bowel cancer screening, bowel cancer
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1772 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Endocuff Vision-assisted Colonoscopy
Arm Type
Active Comparator
Arm Description
Participants in this arm undergo Endocuff Vision-assisted colonoscopy
Arm Title
Standard Colonoscopy
Arm Type
No Intervention
Arm Description
Participants in this arm undergo standard colonoscopy
Intervention Type
Device
Intervention Name(s)
Endocuff Vision
Intervention Description
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).
Primary Outcome Measure Information:
Title
Adenoma detection rate
Description
A difference in adenoma detection rate between Endocuff Vision-assisted colonoscopy and standard colonoscopy.
Time Frame
10 months
Secondary Outcome Measure Information:
Title
Mean adenomas detected per procedure
Description
A difference in mean adenomas detected per procedure between both groups
Time Frame
10 months
Title
Rate of cuff exchange
Description
The rate of cuff exchange (that is, how often the cuff has to be removed) between both groups
Time Frame
10 months
Title
Effect on duration of caecal intubation rates
Description
Duration of complete withdrawal time in procedures where no polyps are detected between both groups
Time Frame
10 months
Title
Patient satisfaction using validated patient comfort Bowel Cancer Screening Programme (BCSP) questionnaires
Description
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).
Time Frame
10 months
Title
Increase in surveillance colonoscopies caused by increased adenoma detection rate
Description
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
Time Frame
10 months
Title
Number of proximal sessile serrated polyps by histology
Description
Number of of proximal sessile serrated polyps in both groups
Time Frame
10 months
Title
Polyp location
Description
Distribution of polyps in the colon in both groups by location
Time Frame
10 months
Title
Adenoma detection rate of BCSP and non-BCSP endoscopists
Description
Adenoma detection rate of BCSP and non-BCSP colonoscopists
Time Frame
10 months
Title
Change in adenoma detection rate of each endoscopist during the course of the trial
Description
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.
Time Frame
10 months
Title
Adenoma detection rate of individual endoscopist before and after trial commencement
Description
Baseline ADR of each colonoscopist prior to trial recruitment with their individual ADR in patients where Endocuff Vision was not used.
Time Frame
10 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
All patients referred for screening, surveillance, or diagnostic colonoscopy
All patients must be able to give informed consent
Exclusion Criteria:
Patients with any absolute contraindications to colonoscopy
Patients with established or suspicion of large bowel obstruction or pseudo-obstruction
Patients with known colon cancer or polyposis syndromes
Patients with known colonic strictures
Patients with known severe diverticular segments (that is likely to impede colonoscope passage)
Patients with active colitis (ulcerative colitis, Crohn's colitis, diverticulitis, infective colitis)
Patients lacking capacity to give informed consent
Pregnancy
Patients who are on clopidogrel, warfarin, or other new generation anticoagulants who have not stopped this for the procedure.
Patients who are attending for a therapeutic procedure or assessment of a known lesion
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wee Sing Ngu, MBChB, MRCS
Phone
01914041000
Ext
2899
Email
wngu@nhs.net
First Name & Middle Initial & Last Name or Official Title & Degree
Gayle Clifford, BSc
Phone
01914041000
Ext
4756
Email
gayle.clifford@stft.nhs.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Colin Rees, MBBS, FRCP
Organizational Affiliation
South Tyneside and Sunderland NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
County Durham and Darlington NHS Foundation Trust
City
Durham
State/Province
County Durham
ZIP/Postal Code
DL3 6HX
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Silcock, MBBS, FRCP
Phone
01325 380100
Email
John.Silcock@cddft.nhs.uk
First Name & Middle Initial & Last Name & Degree
John Silcock, MBBS, FRCP
Facility Name
North Tees and Hartlepool NHS Foundation Trust
City
Stockton-on-Tees
State/Province
County Durham
ZIP/Postal Code
TS19 8PE
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matthew Rutter, MBBS, FRCP
Phone
01642 617617
Email
Matt.rutter@nth.nhs.uk
First Name & Middle Initial & Last Name & Degree
Matthew Rutter, MBBS, FRCP
Facility Name
St Mark's Hospital and Academic Institute
City
Harrow
State/Province
Middlesex
ZIP/Postal Code
HA1 3UJ
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brian Saunders, MBBS, FRCP
Phone
02082354000
Email
b.saunders@imperial.ac.uk
First Name & Middle Initial & Last Name & Degree
Brian Saunders, MBBS, FRCP
Facility Name
South Tees Hospitals NHS Foundation Trust
City
Middlesbrough
State/Province
North Yorkshire
ZIP/Postal Code
TS4 3BW
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arvind Ramadas, MBBS, FRCP
Phone
01642 854860
Email
Arvind.Ramadas@stees.nhs.uk
First Name & Middle Initial & Last Name & Degree
Arvind Ramadas, MBBS,FRCP
Facility Name
Northumbria Healthcare NHS Foundation Trust
City
North Shields
State/Province
Tyne and Wear
ZIP/Postal Code
NE29 8NH
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas Lee, MBBS, FRCP
Phone
0344 811 8111
Email
Tom.Lee@northumbria-healthcare.nhs.uk
First Name & Middle Initial & Last Name & Degree
Thomas Lee, MBBS, FRCP
Facility Name
South Tyneside NHS Foundation Trust
City
South Shields
State/Province
Tyne and Wear
ZIP/Postal Code
NE34 0PL
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wee Sing Ngu, MBChB, MRCS
Phone
01914041000
Ext
2899
Email
wngu@nhs.net
First Name & Middle Initial & Last Name & Degree
Gayle Clifford, BSc
Phone
01914041000
Ext
4756
Email
gayle.clifford@stft.nhs.uk
First Name & Middle Initial & Last Name & Degree
Colin Rees, MBBS, FRCP
Facility Name
City Hospitals Sunderland NHS Foundation Trust
City
Sunderland
State/Province
Tyne and Wear
ZIP/Postal Code
SR4 7TP
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Painter, MBBS, FRCP
Phone
0191 565 6256
Email
John.Painter@chsft.nhs.uk
First Name & Middle Initial & Last Name & Degree
John Painter, MBBS, FRCP
12. IPD Sharing Statement
Citations:
PubMed Identifier
29363535
Citation
Ngu WS, Bevan R, Tsiamoulos ZP, Bassett P, Hoare Z, Rutter MD, Clifford G, Totton N, Lee TJ, Ramadas A, Silcock JG, Painter J, Neilson LJ, Saunders BP, Rees CJ. Improved adenoma detection with Endocuff Vision: the ADENOMA randomised controlled trial. Gut. 2019 Feb;68(2):280-288. doi: 10.1136/gutjnl-2017-314889. Epub 2018 Jan 23.
Results Reference
derived
Learn more about this trial
Accuracy of Detection Using ENdocuff Optimisation of Mucosal Abnormalities
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