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A Study to Test the Repeatability and Reproducibility in Rod Intercept Time Within the AdaptDx Pro in Healthy Subjects With Normal Vision (FlashForward)

NCT07860905

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • No Disease

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
22 to 49 years
Sex
All
Healthy volunteers
Accepted
Sponsor
AdaptDx, Inc.
Last updated on ClinicalTrials.gov
October 6, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Washington · 1

  • Pacific NorthWest Retina (Silverdale) · Silverdale, WA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.