Effectiveness of Using the Speedometer During Colonoscopy
Primary Purpose
Colonic Polyp, Colonic Adenoma, Adenoma Colon
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Speedometer
Sponsored by
About this trial
This is an interventional diagnostic trial for Colonic Polyp focused on measuring Colonoscopy, Adenoma detection rate, Withdrawal time, Artificial Intelligence
Eligibility Criteria
Inclusion Criteria:
- Both women and men aged 18 years or older undergoing colonoscopy for any indication at Beth Israel Deaconess Medical Center (BIDMC), Boston, USA.
Exclusion Criteria:
- Known colorectal cancer, hereditary colorectal polyposis, inflammatory bowel disease, or past history of colectomy.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Colonoscopy with the speedometer
Colonoscopy without the speedometer
Arm Description
Outcomes
Primary Outcome Measures
Withdrawal time
Withdrawal time difference between colonoscopies done without the speedometer (control period) and colonoscopies done with the speedometer (intervention period).
Secondary Outcome Measures
Adenoma detection rate (ADR)
Adenoma detection rate (ADR) of the participating endoscopists during the control period and the intervention period.
Quality of colonoscopy
Proportion of colonoscopies with withdrawal time ≥ 6 minutes.
Full Information
NCT ID
NCT04710251
First Posted
January 11, 2021
Last Updated
January 12, 2021
Sponsor
Norwegian Department of Health and Social Affairs
Collaborators
Beth Israel Deaconess Medical Center, Oslo University Hospital, University of Oslo, Showa University
1. Study Identification
Unique Protocol Identification Number
NCT04710251
Brief Title
Effectiveness of Using the Speedometer During Colonoscopy
Official Title
Effectiveness of Using the Speedometer During Colonoscopy: a Prospective, Comparative Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2021 (Anticipated)
Primary Completion Date
June 30, 2021 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian Department of Health and Social Affairs
Collaborators
Beth Israel Deaconess Medical Center, Oslo University Hospital, University of Oslo, Showa University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
PURPOSE OF PROTOCOL
Objective:
To evaluate if the speedometer based on the real-time image analysis can help endoscopists increase their withdrawal time, which is defined as time spent examining the colon during withdrawal of the colonoscope, during colonoscopy.
Hypothesis:
The trial hypothesis is that use of the speedometer during colonoscopy will increase the average withdrawal time, which is defined as time spent examining the colon during withdrawal of the colonoscope, by 1.6 minutes, possibly increasing the performance of the participating endoscopists. Our objective is to clarify the clinical benefits of this digital tool in colonoscopy.
Endpoint: Withdrawal time difference between colonoscopies done without the speedometer (control period) and colonoscopies done with the speedometer (intervention period).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colonic Polyp, Colonic Adenoma, Adenoma Colon
Keywords
Colonoscopy, Adenoma detection rate, Withdrawal time, Artificial Intelligence
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
332 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Colonoscopy with the speedometer
Arm Type
Active Comparator
Arm Title
Colonoscopy without the speedometer
Arm Type
No Intervention
Intervention Type
Device
Intervention Name(s)
Speedometer
Intervention Description
We will measure and monitor the withdrawal time of colonoscopy with a speedometer.
Primary Outcome Measure Information:
Title
Withdrawal time
Description
Withdrawal time difference between colonoscopies done without the speedometer (control period) and colonoscopies done with the speedometer (intervention period).
Time Frame
Through study completion, an average of 1 year
Secondary Outcome Measure Information:
Title
Adenoma detection rate (ADR)
Description
Adenoma detection rate (ADR) of the participating endoscopists during the control period and the intervention period.
Time Frame
Through study completion, an average of 1 year
Title
Quality of colonoscopy
Description
Proportion of colonoscopies with withdrawal time ≥ 6 minutes.
Time Frame
Through study completion, an average of 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Both women and men aged 18 years or older undergoing colonoscopy for any indication at Beth Israel Deaconess Medical Center (BIDMC), Boston, USA.
Exclusion Criteria:
Known colorectal cancer, hereditary colorectal polyposis, inflammatory bowel disease, or past history of colectomy.
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effectiveness of Using the Speedometer During Colonoscopy
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