Macular Edema, Macular Degeneration
Conditions
Keywords
Age-Related Macular Degeneration, macular edema, retinal vein occlusion, diabetic macular edema
Brief summary
Evaluate the ability and accuracy of the Retinal Health Monitoring System - Retinal Thickness Module (RHMS - RTM).
Detailed description
Evaluation of the Retinal Health Monitoring System - Retinal Thickness Module in subjects with normal macular thickness and subjects with center-involving macular edema.
Interventions
Sponsors
Kubota Vision Inc.
Study design
Observational model
OTHER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
1. Age ≥50. 2. Corrected visual acuity (VA) of 20/125 or better, in the study eye(s) 3. Media clarity, undilated pupil size, and subject cooperation sufficient to obtain adequate OCT B-scans in the study eye(s) 4. Able to perform self-testing of retinal thickness with the RHMS-RTM after training 5. Able and willing to provide written informed consent before undergoing any study-related procedures 6. Group 1: Macula with normal thickness \[central subfield thickness (CST): \<305μm in women, and \<320μm in men as measured by Heidelberg Spectralis SD-OCT in at least one eye. Patients diagnosed with dry AMD are eligible for enrollment into Group 1. No history of wAMD, DR, or RVO in either eye 7. Group 2 and Group 3, in at least one and the same eye: History of center-involving macular edema due to wAMD (Group 2); or DR or RVO (Group 3); Macular edema on SD-OCT with CST ≥305 μm in women, and ≥320μm in men as measured by Heidelberg Spectralis SD-OCT.
Exclusion criteria
1. History of corneal refractive surgery \[e.g., laser-assisted in situ keratomileusis (LASIK), photorefractive keratectomy (PRK), radial keratotomy (RK)\] in the study eye(s) 2. History of epiretinal membrane, vitreomacular traction, or macular hole in the study eye(s) 3. Participation in any study using an investigational drug within 30 days of screening or an investigational device within 60 days of screening 4. Refractive error within defined limits 5. History of photocoagulation laser scar or other retinal scar in the central 3 mm of the macula, in the study eye(s)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Evaluation of the RHMS-RTM retinal thickness measurements | 1 day | To evaluate the ability of the RHMS-RTM device to measure retinal thickness |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Repeatability of RHMS-RTM retina thickness measurements | 1 day | To assess repeatability of the RHMS-RTM device |
| Comparison of retinal thickness measurements between the RHMS-RTM and the SD-OCT | 1 day | To evaluate the agreement of measurements by the RHMS-RTM and SD-OCT |
| Intraretinal and subretinal fluid detection | 1 day | To evaluate the feasibility of intra- and sub-retinal fluid detection |
Countries
Switzerland
Outcome results
None listed