Adenoma Detection Rate Using Endocuff Vision in China (SinoEVADR)
Primary Purpose
Colorectal Neoplasms, Colonic Polyp, Adenoma
Status
Suspended
Phase
Not Applicable
Locations
China
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
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
- Sixth affiliated Hospital, Sun Yat-Sen University
- Shanghai Zhongshan Hospital
- Changhai Hospital
- Tianjin Nankai Hospital
- Tianjin People's Hospital
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, ADR
ADR refer to the rate of adenoma detection, calculated as the proportion of subjects with at least one adenoma.
Secondary Outcome Measures
Polyp detection rate, PDR
PDR refer to the rate of polyp detection, calculated as the proportion of subjects with at least one polyp.
Full Information
NCT ID
NCT03839277
First Posted
February 11, 2019
Last Updated
September 24, 2020
Sponsor
Changhai Hospital
Collaborators
Sixth Affiliated Hospital, Sun Yat-sen University, Shanghai Zhongshan Hospital, Tianjin People's Hospital, Tianjin Nankai Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03839277
Brief Title
Adenoma Detection Rate Using Endocuff Vision in China
Acronym
SinoEVADR
Official Title
Adenoma Detection Rate Using Endocuff Vision in China
Study Type
Interventional
2. Study Status
Record Verification Date
September 2020
Overall Recruitment Status
Suspended
Why Stopped
One investigator is out-of-service due to carrying out another task.
Study Start Date
June 12, 2019 (Actual)
Primary Completion Date
December 1, 2020 (Anticipated)
Study Completion Date
December 1, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Changhai Hospital
Collaborators
Sixth Affiliated Hospital, Sun Yat-sen University, Shanghai Zhongshan Hospital, Tianjin People's Hospital, Tianjin Nankai Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The primary aim of this study is
- to explore the usefulness of Endocuff Vision in colonoscopy on adenoma detection rate (ADR).
Other aims include to explore the data below when Endocuff Vision is used.
Mean adenomas detected per procedure, MAP Proximal Adenoma detection rate, pADR Polyp detection rate, PDR Proximal polyp detection rate, pPDR Mean polyps detected per procedure, MPP Withdrawal time, WT Cecal intubation rate, CIR Cecal intubation time, CIT
Detailed Description
Colorectal cancer is common in China. Most colorectal cancers happen when an adenoma becomes cancerous. Doctors use colonoscopy to look inside the colon and rectum and find adenomas and remove them. Removing adenomas is known to reduce the chances of a person developing colorectal cancers. The ability of colonoscopists finding adenomas varies, and there is a lot of researches into how to improve "adenoma detection rates".
A new device, called the Endocuff Vision has been shown to improve the rate of polyp detection at colonoscopy, and to make polyp removal easier. Previous 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 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 will be invited in 5 centres, recruiting a total of 1200 participants.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Neoplasms, Colonic Polyp, Adenoma
Keywords
adenoma detection rate
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model 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).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1200 (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 attached to the tip of colonoscope before intubation.
Primary Outcome Measure Information:
Title
Adenoma detection rate, ADR
Description
ADR refer to the rate of adenoma detection, calculated as the proportion of subjects with at least one adenoma.
Time Frame
At the end of the procedure, up to 1 hour.
Secondary Outcome Measure Information:
Title
Polyp detection rate, PDR
Description
PDR refer to the rate of polyp detection, calculated as the proportion of subjects with at least one polyp.
Time Frame
At the end of the procedure, up to 1 hour.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
80 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
En-Da YU
Organizational Affiliation
Changhai Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sixth affiliated Hospital, Sun Yat-Sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510655
Country
China
Facility Name
Shanghai Zhongshan Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200032
Country
China
Facility Name
Changhai Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200433
Country
China
Facility Name
Tianjin Nankai Hospital
City
Tianjin
State/Province
Tianjin
ZIP/Postal Code
300100
Country
China
Facility Name
Tianjin People's Hospital
City
Tianjin
State/Province
Tianjin
ZIP/Postal Code
300121
Country
China
12. IPD Sharing Statement
Plan to Share IPD
No
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
background
Links:
URL
http://www.ncbi.nlm.nih.gov/pubmed/29363535
Description
PubMed link
Learn more about this trial
Adenoma Detection Rate Using Endocuff Vision in China
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