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NCT07168564 · ClinicalTrials.gov registry record · NA
Post Marketing Clinical Study on the Efficacy of Lenses From a New Prescription Protocol
A NA study of Ametropia and Refractive Error, sponsored by Essilor International.
- Recruiting
- Registry status
- NA
- Development phase
- 120
- Enrollment target
- 1
- Study location
NCT07168564 is a NA study of Ametropia and Refractive Error that is actively recruiting participants, run by Essilor International. The registered enrollment target is 120 participants, roughly in line with the 131-participant average among 5 other Ametropia trials with a reported enrollment target. The trial reports 1 study location across 1 state.
The verdict
NCT07168564, a NA study of Ametropia and Refractive Error, is actively recruiting participants, sponsored by Essilor International.
- RECRUITING
- Registry status
- NA
- Development phase
- 120 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to assess improvements in visual performance and patient outcomes in wearing new spectacle lenses in general population. The two spectacle lenses will be compared after two weeks of wearing. The aims are: * to evaluate the visual superiority, and quality-of-life implications of Essilor® AVA™ spectacle lenses prescribed after a new subjective refraction protocol named AVA™ protocol. * to understand the benefits of using a high accuracy instrument and testing sequence over the standard testing sequence in determining a glasses prescription, as well as the overall subjective performance of the resulting glasses.
Conditions Studied
Interventions
- DEVICE AVA lenses
- DEVICE Standard lenses
Study Locations (1)
Indiana
- Clinical Optics Research Lab @ Borish Center for Ophthalmic Research Indiana University School of Optometry Indiana University - Bloomington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2025-09-22 |
| Est. Completion | 2026-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07168564
The ClinicalTrials.gov registry entry for NCT07168564 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 131-participant average among 5 other Ametropia trials with a reported enrollment target. The listed sponsor is Essilor International, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Ametropia appearing as the primary indexed condition, and to 2 interventions - of which AVA lenses is the first listed.
NCT07168564 reports 1 study location spanning 1 distinct geographic area - top geographies include Indiana.
Frequently Asked Questions
What is clinical trial NCT07168564 about?
NCT07168564 is a clinical study titled "Post Marketing Clinical Study on the Efficacy of Lenses From a New Prescription Protocol". The goal of this clinical trial is to assess improvements in visual performance and patient outcomes in wearing new spectacle lenses in general population. The two spectacle lenses will be compared after two weeks of wearing. The aims are: * to evaluate the visual superiority, and quality-of-life...
What is the current status of trial NCT07168564?
This trial is currently recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2025-09-22. Estimated completion is 2026-01.
What conditions does trial NCT07168564 study?
This clinical trial studies the following conditions: Ametropia, Refractive Error.
What interventions are being tested in trial NCT07168564?
The interventions under investigation include: AVA lenses (DEVICE), Standard lenses (DEVICE).
Who is sponsoring clinical trial NCT07168564?
This trial is sponsored by Essilor International, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07168564 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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