Optos P200TE Agreement and Precision Study
Completed · Not applicable
Conditions studied: Retinal Disease, Glaucoma
In brief
This study is a prospective comparative, randomized, single center study to assess agreement and precision of the Optos P200TE in comparison to the predicate device in normal subjects, subjects with glaucoma, and subjects with retinal disease.
Key facts
- Study ID
- NCT03868462
- Run by
- Optos, PLC
- People needed
- 137
- Starts
- 2019-02-11
- Expected to finish
- 2019-09-16
- Last updated by the study team
- 2019-10-15
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: accepted.
Where it is running
- New England Retina Consultants — Springfield, Massachusetts, United States
Full record on ClinicalTrials.gov
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