A Study to Understand the Usage of an Artificial Intelligence Technology Called DARWEN for Eye Disorders and to Find Out the Factors Influencing Treatment Frequencies in People With nAMD and RVO
NCT ID: NCT06495203
Last Updated: 2024-07-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
1350 participants
OBSERVATIONAL
2023-11-02
2024-02-29
Brief Summary
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Neovascular age-related macular edema (nAMD): an eye disorder caused by the lack of oxygen in the retina. The lack of oxygen leads to the increase of a protein called vascular endothelial growth factor (VEGF). VEGF causes new, weak blood vessels to grow. These vessels can leak fluid or blood into the central part of the retina at the back of the eye (macula). This leads to blurring or a blind spot in the central (straight ahead) vision needed for reading or threading a needle.
Retinal vein occlusion (RVO): an eye disorder where a blood vessel that carries blood away from the retina (vein) becomes blocked. The blocked vein causes a lack of oxygen in the retina which leads to the increase of VEGF and then vision disturbances.
These eye disorders can be treated with a type of medicine called anti-vascular endothelial growth factor (anti-VEGF). Anti-VEGF treatment helps control the growth of new blood vessels in the eye and is given via injection into the eye.
DARWEN AI is a system using artificial intelligence (AI) technology. It has been proven that DARWEN AI can be used to extract data accurately and efficiently in multiple disease areas, including breast cancer, lung cancer, ambulatory care diseases and skin disorders.
The main purpose of this study is to validate if DARWEN AI can extract and sort through information from participants' health records accurately to identify those who need more frequent injections and those who do not.
The secondary purpose of this study is to use DARWEN AI to describe the factors influencing treatment frequencies in participants with nAMD or influencing treatment discontinuation in participants with RVO.
The data will come from the participants' information stored in EyeDoc Electronic Medical Records (EMR) at St. Joseph Health Care in London. Data collected are from January 1, 2009, to May 31, 2023.
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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nAMD patients, anti-VEGF naïve on treatment after July 2015
* Cluster A: Likely to require frequent injections
* Cluster B: Probable to extend treatment interval
* Cluster C: Likely to extend treatment interval
anti-VEGF treatment
Follow clinical practice/administration
nAMD patients, anti-VEGF naïve on treatment before July 2015
* Cluster D: Likely to require frequent injections
* Cluster E: Probable to extend treatment interval
* Cluster F: Likely to extend treatment interval
anti-VEGF treatment
Follow clinical practice/administration
nAMD patients, anti-VEGF experienced on treatment after July 2015
* Cluster G: Likely to require frequent injections
* Cluster H: Likely to extend treatment interval
anti-VEGF treatment
Follow clinical practice/administration
CRVO patients, anti-VEGF naïve on treatment after July 2015
* Cluster A: Likely to require continued anti-VEGF treatment
* Cluster B: Likely to be off anti-VEGF treatment
anti-VEGF treatment
Follow clinical practice/administration
BRVO patients, anti-VEGF naïve on treatment after March 2017
* Cluster C: Likely to require continued anti-VEGF treatment
* Cluster D: Likely to be off anti-VEGF treatment
anti-VEGF treatment
Follow clinical practice/administration
Interventions
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anti-VEGF treatment
Follow clinical practice/administration
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Bayer
INDUSTRY
Responsible Party
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Locations
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Bayer
Mississauga, , Canada
Countries
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Related Links
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Click here for access to information about Bayer's transparency standards and Bayer studies.
Other Identifiers
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22642
Identifier Type: -
Identifier Source: org_study_id
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