Evaluation of Novel Spectacles Intended for Myopia Management in a Short-Term Study
ConditionMyopia: Refractive Error
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-15
SponsorMyoptechs, Inc
About this trial
The primary objective of this study is to evaluate the visual acuity, wearability, and quality of vision with two novel multifocal glasses designs in habitual myopia control glasses wearers, in a non-dispensing study after short-term wear.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
8 - 15 years of age, inclusive.
Ability of the child to assent, and for one parent to provide permission to participate.
Had an eye examination within the past year.
Distance visual acuity of 20/25 (logMAR +0.10) or better in each eye with best corrected with sph/cyl subjective refraction.
Disqualifiers
Current report of active ocular inflammation or infection.
Astigmatism > 1.00 D in either eye
History of previous eye surgery
Trial design
Design model
Crossover
Treatments tested in this trial
Habitual myopia glasses
DeviceHabitual myopia glasses of study P/905/25/MO
Myopia Glasses A
DeviceMyopia glasses A of study P/905/25/MO
Myopia Glasses B
DeviceMyopia glasses B of study P/905/25/MO
Treatment groups
20 Participants
are divided into 3 treatment groupsGroup A: Habitual myopia glassesActive comparator 1 intervention
Group B: Myopia Glasses AExperimental treatment 1 intervention
Group C: Myopia Glasses BExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Binocular visual acuity
Binocular visual acuity with habitual myopia spectacle lens design and two test spectacle lens designs.
Time frame
20 minutes of wearing each lens design.Locations
Sponsors and contacts
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Myoptechs, Inc
Lead sponsor
University of Waterloo School of Optometry and Vision Science
Collaborator
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: