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NCT03608150 · ClinicalTrials.gov registry record · NA

Luminopia One Amblyopia Vision Improvement Study

A NA study, sponsored by Luminopia.

Completed
Registry status
NA
Development phase
117
Enrollment target

NCT03608150: Completed NA study, sponsored by Luminopia.

NCT03608150 is a NA study that has completed, run by Luminopia. The registered enrollment target is 117 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03608150, a NA study, has completed, sponsored by Luminopia.

COMPLETED
Registry status
NA
Development phase
117 participants
Enrollment target

Study Summary

The objective of the study is to demonstrate the safety and efficacy of Luminopia One in amblyopia patients with amblyopia associated with anisometropia and/or with mild strabismus.

Primary Outcome

Mean improvement in best-corrected visual acuity of amblyopic eye from baseline after 12 weeks of treatment using electronic ATS-HOTV protocol.

Interventions

  • DEVICE Luminopia One
  • DEVICE Refractive Correction

Trial Details

FieldValue
Enrollment Target 117 participants
Start Date 2019-01-16
Est. Completion 2020-07-31
Phase NA
Luminopia

3 total trials

What the finished NCT03608150 record still lists

NCT03608150 is an interventional study that assigns participants to a tested intervention. The registered 117 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 2 interventions - of which Luminopia One is the first listed.

NCT03608150 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03608150 about?

NCT03608150 is a clinical study titled "Luminopia One Amblyopia Vision Improvement Study". The objective of the study is to demonstrate the safety and efficacy of Luminopia One in amblyopia patients with amblyopia associated with anisometropia and/or with mild strabismus.

What is the current status of trial NCT03608150?

This trial is currently completed. It is a NA study. The enrollment target is 117 participants. The study started on 2019-01-16. Estimated completion is 2020-07-31.

What interventions are being tested in trial NCT03608150?

The interventions under investigation include: Luminopia One (DEVICE), Refractive Correction (DEVICE).

Who is sponsoring clinical trial NCT03608150?

This trial is sponsored by Luminopia, which has 3 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03608150's enrollment target sits among peer trials

117 807th of 2000 higher than 1,193 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03608150, the US trial registry maintained by the National Library of Medicine. NCT03608150 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.