Ignite Creation Date:
2024-05-06 @ 7:03 PM
Last Modification Date:
2024-10-26 @ 2:59 PM
Study NCT ID:
NCT05870332
Status:
RECRUITING
Last Update Posted:
2024-03-06
First Post:
2023-05-02
Brief Title:
Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy
Sponsor:
Kings College Hospital NHS Trust
Organization:
Kings College Hospital NHS Trust
Study Overview
Official Title:
Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy
Status:
RECRUITING
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
NAIAD
Brief Summary:
The goal of this trial is to determine whether use of a Computer Assisted Detection CADe programme leads to an increase in ADR for either units or individual colonoscopists independent of setting or expertise
Detailed Description:
This is a case-control study comparing adenoma detection rate ADR in hospitals and individual colonoscopists before during and after use with an artificial intelligence unit called GI Genius GIG GIG is a Computer-assisted detection CADe module that assists the human colonoscopist in real-time by detecting and marking out polyps during colonoscopy It has been shown to be effective in expert colonoscopists but the effect in non-expert general colonoscopists is not known
The investigator wish to deploy GIG into colonoscopy through the UK using a step-wedge design Sites will be randomly allocated a start date for GIG deployment collecting data for four months prior to this In this way all sites will have the active intervention and will provide their own case-control data 4 months collection prior to activating GIG 4 months with GIG 4 months afterwards without GIG
The study will concentrate on non-expert colonoscopists to determine whether GIG can increase ADR Patients will undergo the same colonoscopy that they would have had in any case with no additional trial visits or interventions There will be no alteration to the usual care pathway from the patients perspective
If the investigator can prove GIG increases ADR in this way it will provide support to roll out this technology routinely to improve the quality of colonoscopy nationwide
The investigator wish to deploy GIG into colonoscopy through the UK using a step-wedge design Sites will be randomly allocated a start date for GIG deployment collecting data for four months prior to this In this way all sites will have the active intervention and will provide their own case-control data 4 months collection prior to activating GIG 4 months with GIG 4 months afterwards without GIG
The study will concentrate on non-expert colonoscopists to determine whether GIG can increase ADR Patients will undergo the same colonoscopy that they would have had in any case with no additional trial visits or interventions There will be no alteration to the usual care pathway from the patients perspective
If the investigator can prove GIG increases ADR in this way it will provide support to roll out this technology routinely to improve the quality of colonoscopy nationwide
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None