Ophthalmopathy Clinical Trial
Official title:
Artificial Intelligence Screening on Patients With Primary Angle Closure Glaucoma
The Tomey CASIA (Tomey Corporation, Nagoya, Japan) is a novel rapid imaging device that captures high-quality imaging of the entire anterior chamber of the eye over detailed imaging of a single section. In this prospective study, we want to investigate and compare the anatomical structure of the drainage angle of the eye in patients with different types glaucoma using Tomey machine. This study gives us a better understanding of the predictability, validity and accuracy of Tomey machine in the diagnosis of different types of glaucoma. Moreover, the data collected here will be used to create an artificial intelligence (AI) platform to screen certain type of glaucoma.
Patients ≥18 years old from ophthalmic clinics with or without glaucoma were enrolled to this respective observational clinical study. However, patients with any history of eye surgery (except cataract surgery) including laser procedure were excluded. The investigators will review patients' medical chart and update any medical history in your medical record. If new scans are needed, investigators will do them at the time of patients' current visit and it will require about 30 mins. CASIA SS-OCT (CASIA 2) is a non-contact scan of the front of the eye with higher resolution and provides deeper, wider and three- dimensional views. It is the newest scan machine. It is not FDA-approved but is approved in many other countries including Japan for patient use. We may perform the scan in the light and dark condition. We may also perform the routine scan to capture images of the anterior part of the eye for comparison purpose. The results of the scanned data will be among patients' medical records. Age, sex and ethnicity within your medical records will also be used for the analysis. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05414994 -
Assessment of the Ocular Microbiome in Health and Disease
|
||
Completed |
NCT04387292 -
Ocular Sequelae of Patients Hospitalized for Respiratory Failure During the COVID-19 Epidemic
|
N/A | |
Completed |
NCT05494242 -
Single Superior ILM/ERM Flap for the FTMH.
|
N/A | |
Terminated |
NCT05494229 -
Autologous Blood for Full-thickness Macular Hole
|
N/A | |
Completed |
NCT04982484 -
Reading Speed Improvements in Wet-AMD Patients After Ranibizumab Treatment
|
||
Completed |
NCT04683055 -
Phaco-Trabeculotomy Vs Phaco-Trabeculectomy
|
N/A | |
Recruiting |
NCT06367517 -
Tocilizumab in Corticosteroid-Resistant Graves' Orbitopathy (Thyroid Eye Disease)
|
||
Completed |
NCT03766737 -
Validation of the Utility of an Intelligent Visual Acuity Diagnostic System for Children
|
N/A | |
Recruiting |
NCT04460001 -
Injection of Ranibizumab Versus Combination of Ranibizumab and Triamcinolone Acetate for (CRVO)
|
Phase 2/Phase 3 | |
Completed |
NCT04917562 -
Refractive Transepithelial Photo-keratectomy (T-PKR) in High Myopia
|
||
Completed |
NCT04771039 -
Ocular Manifestations of Inflammatory Bowel Disease
|
||
Completed |
NCT03492242 -
Immune CHeckpoint Inhibitors Monitoring of Adverse Drug ReAction
|
||
Withdrawn |
NCT04579458 -
Assessment of COVID-19 in Tearfilm
|
||
Completed |
NCT03855462 -
Evaluating Medium-chain Triglycerides as a Temporary Intraocular Tamponading Agent for Retinal Detachment
|
N/A | |
Recruiting |
NCT06293586 -
Comparison Between Peribulbar And Sub-tenon Blocks on Oculocardiac Reflex (OCR) During Pediatric Strabismus Surgery
|
N/A | |
Recruiting |
NCT06102265 -
Effect Of Reusing the Operative Supplies On Cataract Surgery and Climate Change
|
||
Completed |
NCT03499145 -
Validation of the Utility of Ophthalmology Intelligent Diagnostic System
|