P200TE Agreement and Precision Study

Stopped early · Not applicable

Conditions studied: Retina Disease, Glaucoma, Normal

In brief

This study is a prospective comparative, randomized, single center study to assess agreement and precision of the P200TE in comparison to the predicate device in normal subjects, subjects with glaucoma, and subjects with retinal disease.

Key facts

Study ID
NCT05536401
Run by
Optos, PLC
People needed
15
Starts
2022-09-02
Expected to finish
2022-09-20
Last updated by the study team
2022-11-17

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: accepted.

Where it is running

Full record on ClinicalTrials.gov

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