AdaptDx, Inc.
The purpose of this study is to test the repeatability and reproducibility in Rod Intercept (RI) time with two AdaptDx Pro devices in healthy subjects with normal vision.
This study is a prospective, single-center study to test the repeatability and reproducibility in Rod Intercept (RI) time with two AdaptDx Pro devices in healthy subjects with normal vision. Sixteen subjects will be enrolled. Both eyes will be evaluated.
Inclusion Criteria (each eye qualifies for the study independently): 1. Male or female between the ages of 22 and 49 (inclusive) at Visit 1 2. ETDRS BCVA letter score of 85 (Snellen equivalent of 20/20) or better at Visit 1 3. Able to communicate well with the Investigator and able to understand and comply with the requirements of the study 4. Informed of the nature of this study and has provided written informed consent in accordance with institutional, local and national regulatory guidelines Exclusion Criteria (each eye qualifies for the study independently): 1. Unable to follow simple i…
The AdaptDx device measures changes in dark adaptation via rod intercept time.
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