A Study to Test the AdaptDx Pro Agreement in Rod Intercept Time With the AdaptDx in Healthy Subjects With Normal Vision (FlashBack)

Part of paid clinical trials in San Diego, California.

Sponsor
AdaptDx, Inc.
Study ID
NCT07803588
Status
Recruiting
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Conditions

  • Healthy Adult Participants

Eligibility Criteria

Sex
ALL
Age
22 Years - 49 Years
Healthy Volunteers
Accepted

Interventions

  • AdaptDx Tabletop vs AdaptDx Pro — DIAGNOSTIC_TEST
    Two variations of AdaptDx dark adaptation devices.

Study Details

The purpose of this study is to test the AdaptDx Pro agreement in Rod Intercept (RI) time with the AdaptDx tabletop (AdaptDx) in healthy subjects with normal vision.

Key Dates

First listed
Sep 3, 2026
Start date
Sep 15, 2026
Status verified
Sep 2026
Primary completion
Jan 1, 2027
Completion
Mar 1, 2027

Study Design

Enrollment
24 participants (estimated)

Arms

  • Arm: AdaptDx Tabletop
    Rod intercept time will be measured using the AdaptDx Tabletop device
  • Arm: AdaptDx Pro Wearable
    Rod intercept time will be measured using the AdaptDx Pro device

Primary Outcome Measure

Rod Intercept Time [ Time Frame: Immediately after the dark adaptation test ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Retina Consultants San DiegoSan DiegoCalifornia92101
Nikolas London, MD, FACS
[email protected]
858-451-1911

Find similar trials in San Diego, CA

By research site
Retina Consultants San Diego· San Diego, CA

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