- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04478929
Early Detection of Barrett's Esophagus Through Deep Image Retrieval
Early Detection of Cancer in Cases of Barrett's Esophagus Using Robotic Endoscopy Image Analysis Through Deep Image Retrieval
Study Overview
Detailed Description
The project intention is to acquire secondary endoscopy captured data from clinicians to create a sufficient dataset to train a learning system to achieve the stated objective. The data required will feature footage (images/videos) from inside the oesophagus. The preferred data would contain associated diagnosis notes and description, however, data without diagnosis can still be used. All data can and will be anonymised, as personal information will not be useful in this work.
The data will be labelled by either researchers, or professional clinicians and prepared ready to feed into a chosen learning AI system. Through an iterative learning process, the chosen AI system will learn to discriminate between severity of Barrett's oesophagus and output optimal biopsy target.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Lyndon Winstone, PhD
- Phone Number: +4411732 82009
- Email: Lyndon.Smith@uwe.ac.uk
Study Contact Backup
- Name: benjamin winstone, PhD
- Phone Number: 07890080486
- Email: benjamin2.winstone@uwe.ac.uk
Study Locations
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Avon
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Bristol, Avon, United Kingdom, BS10 5NB
- NBT, Southmead Hospital
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Contact:
- leonard griffiths
- Phone Number: 6353 0117 414 6353
- Email: leonard.griffiths@nbt.nhs.uk
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult
- Attending Southmead Hospital for on OGD
- Has capacity
- Initially any indication, later patients with known Barrett's oesophagus
Exclusion Criteria:
- Children (<18)
- Patients without capacity
- Urgent and emergency procedures
- Limited English
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
gastroscopy clinic patients
NBT gastroscopy clinic invited participants.
Patients are already due to attend the clinic, and we are inviting them to share their gastroscopy data with our research study.
|
Routine gastroscopy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
gastroscopy image data set
Time Frame: 12 months
|
Images collected during routine gastroscopy with examination notes
|
12 months
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REDM0227_RP01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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