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AmplifEYE Colonoscopy vs Standard Colonoscopy

Primary Purpose

Colon Polyp, Adenoma Colon, Serrated Polyp

Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
AmplifEYE
Sponsored by
Queen Elizabeth Hospital, Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Colon Polyp focused on measuring colonoscopy, adenoma detection rate, colorectal cancer screening, new technology

Eligibility Criteria

50 Years - 79 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Aged between 50 to 79 years old
  • Scheduled for screening, surveillance or diagnostic colonoscopy

Exclusion Criteria:

  • Colonic strictures
  • History of bowel surgery
  • Per-rectal bleeding within six weeks
  • Inflammatory bowel disease
  • Pregnancy

Sites / Locations

  • Department of Medicine, Queen Elizabeth Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

AmplifEYE colonoscopy

Standard colonoscopy

Arm Description

Colonoscopy performed with AmplifEYE equipped

Standard colonoscopy performed

Outcomes

Primary Outcome Measures

Adenoma detection rate
number of patients in whom at least one adenoma could be found

Secondary Outcome Measures

Polyp detection rate
number of patients in whom at least one polyp could be found
Serrated polyp detection rate
number of patients in whom at least one serrated polyp could be found
caecal intubation rate
number of patients in whom caecal intubation is acheived
caecal intubation time
time beginning with the insertion of the colonoscope until reaching the caecum

Full Information

First Posted
January 20, 2019
Last Updated
March 24, 2019
Sponsor
Queen Elizabeth Hospital, Hong Kong
Collaborators
Our Lady of Maryknoll Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03814369
Brief Title
AmplifEYE Colonoscopy vs Standard Colonoscopy
Official Title
Use of AmplifEYE-assisted Colonoscopy Compared to Standard Colonoscopy in Polyp and Adenoma Detection
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
March 1, 2017 (Actual)
Primary Completion Date
June 30, 2018 (Actual)
Study Completion Date
November 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Queen Elizabeth Hospital, Hong Kong
Collaborators
Our Lady of Maryknoll Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Colonoscopy screening is proven to reduce mortality rates for colorectal cancer, which relies on early detection and removal of colonic polyps. AmplifEYE is a FDA-approved device with a row of flexible detection arms attached to the tip of colonoscope which can separate colonic folds during scope withdrawal and is believed to improve polyp detection. Real-life clinical data on this relatively new device is lacking and this study aims to compare the adenoma and polyp detection rates in AmplifEYE-assisted colonoscopy versus standard colonoscopy.
Detailed Description
This is a prospective, randomized controlled study. Patients admitted to Queen Elizabeth Hospital and Our Lady of Maryknoll Hospital for colonoscopy are randomly allocated 1:1 to receive either colonoscopy equipped with AmplifEYE (AC) or standard colonoscopy (SC). All study team members will have a prior run-in phase of performing at least 5 AmplifEYE colonoscopies before starting the study. The colonic polyp detection rate (PDR), adenoma detection rate (ADR), serrated polyp detection rate (SDR), caecal intubation time, colonoscope withdrawal time, procedure pain and any adverse events were analyzed in each group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Polyp, Adenoma Colon, Serrated Polyp, Colonic Neoplasms
Keywords
colonoscopy, adenoma detection rate, colorectal cancer screening, new technology

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
355 (Actual)

8. Arms, Groups, and Interventions

Arm Title
AmplifEYE colonoscopy
Arm Type
Experimental
Arm Description
Colonoscopy performed with AmplifEYE equipped
Arm Title
Standard colonoscopy
Arm Type
No Intervention
Arm Description
Standard colonoscopy performed
Intervention Type
Device
Intervention Name(s)
AmplifEYE
Intervention Description
AmplifEYE colonoscopy
Primary Outcome Measure Information:
Title
Adenoma detection rate
Description
number of patients in whom at least one adenoma could be found
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Polyp detection rate
Description
number of patients in whom at least one polyp could be found
Time Frame
1 day
Title
Serrated polyp detection rate
Description
number of patients in whom at least one serrated polyp could be found
Time Frame
1 day
Title
caecal intubation rate
Description
number of patients in whom caecal intubation is acheived
Time Frame
1 day
Title
caecal intubation time
Description
time beginning with the insertion of the colonoscope until reaching the caecum
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Aged between 50 to 79 years old Scheduled for screening, surveillance or diagnostic colonoscopy Exclusion Criteria: Colonic strictures History of bowel surgery Per-rectal bleeding within six weeks Inflammatory bowel disease Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shun Fung Sze, MBBS
Organizational Affiliation
Department of Medicine, Queen Elizabeth Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Medicine, Queen Elizabeth Hospital
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24047059
Citation
Nishihara R, Wu K, Lochhead P, Morikawa T, Liao X, Qian ZR, Inamura K, Kim SA, Kuchiba A, Yamauchi M, Imamura Y, Willett WC, Rosner BA, Fuchs CS, Giovannucci E, Ogino S, Chan AT. Long-term colorectal-cancer incidence and mortality after lower endoscopy. N Engl J Med. 2013 Sep 19;369(12):1095-105. doi: 10.1056/NEJMoa1301969.
Results Reference
background
PubMed Identifier
8978338
Citation
Rex DK, Cutler CS, Lemmel GT, Rahmani EY, Clark DW, Helper DJ, Lehman GA, Mark DG. Colonoscopic miss rates of adenomas determined by back-to-back colonoscopies. Gastroenterology. 1997 Jan;112(1):24-8. doi: 10.1016/s0016-5085(97)70214-2.
Results Reference
background
PubMed Identifier
24693890
Citation
Corley DA, Jensen CD, Marks AR, Zhao WK, Lee JK, Doubeni CA, Zauber AG, de Boer J, Fireman BH, Schottinger JE, Quinn VP, Ghai NR, Levin TR, Quesenberry CP. Adenoma detection rate and risk of colorectal cancer and death. N Engl J Med. 2014 Apr 3;370(14):1298-306. doi: 10.1056/NEJMoa1309086.
Results Reference
background
PubMed Identifier
20463339
Citation
Kaminski MF, Regula J, Kraszewska E, Polkowski M, Wojciechowska U, Didkowska J, Zwierko M, Rupinski M, Nowacki MP, Butruk E. Quality indicators for colonoscopy and the risk of interval cancer. N Engl J Med. 2010 May 13;362(19):1795-803. doi: 10.1056/NEJMoa0907667.
Results Reference
background
PubMed Identifier
25470133
Citation
Floer M, Biecker E, Fitzlaff R, Roming H, Ameis D, Heinecke A, Kunsch S, Ellenrieder V, Strobel P, Schepke M, Meister T. Higher adenoma detection rates with endocuff-assisted colonoscopy - a randomized controlled multicenter trial. PLoS One. 2014 Dec 3;9(12):e114267. doi: 10.1371/journal.pone.0114267. eCollection 2014.
Results Reference
background
PubMed Identifier
26171436
Citation
Sawatzki M, Meyenberger C, Marbet UA, Haarer J, Frei R. Prospective Swiss pilot study of Endocuff-assisted colonoscopy in a screening population. Endosc Int Open. 2015 Jun;3(3):E236-9. doi: 10.1055/s-0034-1391418. Epub 2015 Feb 27.
Results Reference
background
PubMed Identifier
26674360
Citation
van Doorn SC, van der Vlugt M, Depla A, Wientjes CA, Mallant-Hent RC, Siersema PD, Tytgat K, Tuynman H, Kuiken SD, Houben G, Stokkers P, Moons L, Bossuyt P, Fockens P, Mundt MW, Dekker E. Adenoma detection with Endocuff colonoscopy versus conventional colonoscopy: a multicentre randomised controlled trial. Gut. 2017 Mar;66(3):438-445. doi: 10.1136/gutjnl-2015-310097. Epub 2015 Dec 16.
Results Reference
background

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AmplifEYE Colonoscopy vs Standard Colonoscopy

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