CTRI/2021/07/035145
Not yet recruiting
未知
Validation of Medios AI, an Automated Glaucoma Screening Tool, Deployed Offline, On-The-Edge, on a Smartphone Based Fundus Camera- a prospective Study
Remidio Innovative Solutions Pvt Ltd0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Remidio Innovative Solutions Pvt Ltd
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Glaucoma Group:Any case of glaucoma with typical glaucomatous disc changes, confirmed by clinical evaluation and visual field test (primary open angle glaucoma(POAG), normal tension glaucoma (NTG), primary angle closure glaucoma (PACG), secondary glaucomas)
- •2\.Normal Controls (including Ocular hypertension (OHT) and primary angle closure suspects (PACS) status post laser peripheral iridotomy (LPI))
- •3\.Disc suspects
- •4\.Reliable Visual field (false positive (FP), false negative (FN) \<20%)
Exclusion Criteria
- •1\.Patient with acute or sudden vision loss
- •2\.Patient deemed to have narrow angles on gonioscopy and cannot be dilated (primary angle closure)
- •3\.Co\-existing retinal pathologies precluding view of disc including Proliferative diabetic retinopathy
- •4\.Significant media opacity precluding adequate view of the disc
- •5\. Participant has a condition that, in the opinion of the investigator, would preclude participation in the study (e.g., uncontrolled intraocular pressure, active eye infection, \<3 months post\- glaucoma filtering surgery, unstable medical status including blood pressure or glycemic control).
- •6\.Participant is contraindicated for imaging by fundus imaging systems used in the study:
- •a.Participant is hypersensitive to light
- •b.Participant recently underwent photodynamic therapy (PDT)
- •c.Participant is photosensitive or is consuming medication that causes photosensitivity.
Outcomes
Primary Outcomes
Not specified
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