OCT Agreement and Crossed Precision Study
The purpose of this study is to asses the agreement of the RS-3000 Lite and RS-3000 Advance to the RS-3000, assess the crossed precision of each study device and to assess the transference of a reference database from the RS-3000 to the RS-3000 Lite and to the RS-3000 Advance.
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||Crossed Precision Design Study of the Nidek Optical Coherence Tomography RS-3000, RS-3000 Lite and RS-3000 Advance for the Measurements of Retinal and RNFL Thickness, Optic Disc Analysis, and Pachymetry|
- Retinal thickness [ Time Frame: Approximately four hours ] [ Designated as safety issue: No ]Time frame is the maximum duration of hospital stay
- Optic Disc Analysis [ Time Frame: Approximately four hours ] [ Designated as safety issue: No ]Time frame is the maximum duration of hospital stay
- Corneal Thickness [ Time Frame: Approximately four hours ] [ Designated as safety issue: No ]Time frame is the maximum duration of hospital stay
|Study Start Date:||January 2014|
|Estimated Study Completion Date:||June 2014|
|Estimated Primary Completion Date:||June 2014 (Final data collection date for primary outcome measure)|
Eyes without pathology.
Eyes with Glaucoma.
Eyes with Retinal Disease.
Eyes with corneal disease including a kerato-refractive group.
Please refer to this study by its ClinicalTrials.gov identifier: NCT02050880
|United States, California|
|WCCT Global Opthalmology Research Center||Recruiting|
|Santa Ana, California, United States, 92705|
|Contact: Johnny Leng 312-925-0906 Johnny.Leng@wcct.com|
|Principal Investigator: Michael Sheety, M.D.|