There are currently 20 active clinical trials seeking participants for Myopia research studies. The states with the highest number of trials for Myopia participants are California, Florida, Ohio and Texas.
MiSight 1 Day Safety Post-Approval Study
NCT05285527
Recruiting
The purpose of this post-approval study is to confirm the safety of daily disposable soft contact lens wear among the intended patient population for the MiSight 1 Day lens in the US.
Gender:
ALL
Ages:
Between 8 years and 12 years
Trial Updated:
10/17/2024
Locations: Experts on Sight LLC., Gilbert, Arizona +46 locations
Conditions: Myopia
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MiSight 1 Day Post-Approval Study for Effectiveness and Visual Symptoms
NCT05285553
Recruiting
The purpose of this post-approval study is to confirm the effectiveness of the MiSight 1 Day lens in clinical practices within the US and to assess the stability of the myopia reduction over one-year post-treatment.
Gender:
ALL
Ages:
Between 8 years and 12 years
Trial Updated:
10/17/2024
Locations: University of Alabama School of Optometry, Birmingham, Alabama +29 locations
Conditions: Myopia
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Clinical Applications of Advanced Ophthalmic Imaging
NCT03135327
Recruiting
The purpose of this study is to determine the clinical application of advanced ophthalmic imaging devices such as optical coherence tomography (OCT), retinal function imager (RFI), slit-lamp biomicroscopy (SLB), PERG in diseased eyes and normal controls. There are two phases in this study. The first phase is an observational phase which studies the eye in various conditions. The second phase is an interventional phase which studies the changes in the eyes after taking an over-the-counter medica... Read More
Gender:
ALL
Ages:
Between 18 years and 99 years
Trial Updated:
09/03/2024
Locations: Bascom Palmer Eye Institute, Miami, Florida
Conditions: Multiple Sclerosis, Dry Eye Syndromes, Diabetic Retinopathy, Presbyopia, Myopia, Dementia
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Contoura With Phorcides Compared to Wavefront Optimized LASIK
NCT05486546
Recruiting
Comparing post-operative visual acuity and patient reported satisfaction between Contoura with Phorcides and WaveLight Wavefront Optimized.
Gender:
All
Ages:
Between 21 years and 38 years
Trial Updated:
04/24/2023
Locations: Vance Thompson Vison, Bozeman, Montana +3 locations
Conditions: Myopia, Astigmatism
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Progressive Myopia Treatment Evaluation for NaturalVue Multifocal Contact Lens Trial
NCT05159765
Recruiting
This is a multi-center, randomized, double-masked clinical trial. All study devices are market approved/cleared in the localities where the study is conducted. Subjects will be randomly assigned to wear NaturalVue Sphere single vision contact lenses (SVCL) or NaturalVue Multifocal (NVMF) soft contact lenses for a total of three years.
Gender:
All
Ages:
Between 7 years and 13 years
Trial Updated:
10/03/2022
Locations: Fig Garden Optometry, Fresno, California +7 locations
Conditions: Myopia
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Evaluation of The Comfort of Orthokeratology Lenses Fit Using A New Software
NCT05389072
Recruiting
As new orthokeratology fitting software emerges onto the market, it is of interest to assess their usefulness in guiding eye practitioners with lens fit. The goal of this study is to evaluate the comfort of Paragon orthokeratology lenses when they are fit using the new Procornea software.
Gender:
All
Ages:
Between 6 years and 35 years
Trial Updated:
09/22/2022
Locations: 4S Eyecare and Optometry, San Diego, California +3 locations
Conditions: Myopia
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Binocular Peripheral Myopic Defocus Using a Clinical Prototype Device
NCT05425108
Recruiting
Kubota Vision Inc. has developed a spectacle-like prototype device which is designed to be used as a light-based therapy to reduce myopia progression. In this study, we aim to observe the ocular biometric and refractive changes following binocular part-time wear of the clinical prototype device over a course of 12 months and compare that to 12 months of no clinical prototype device use (control).
Gender:
All
Ages:
Between 7 years and 12 years
Trial Updated:
06/30/2022
Locations: Manhattan Vision Associates/Institute of Vision Research, New York, New York
Conditions: Myopia
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SMILE (Small Incision Lenticule Extraction) in the DoD (Department of Defense)
NCT04072289
Recruiting
The Use of the VisuMaxTM Femtosecond Laser Small-Incision Lenticule Extraction (SMILE) Procedure for the Correction of Myopia with or without Astigmatism study is a prospective, non-randomized, multicenter clinical study that will be conducted by the Navy Refractive Surgery Center, Naval Medical Center San Diego, CA in collaboration with the U.S. Air Force 59th Medical Wing, Wilford Hall Eye Center, TX, and the U.S. Army Warfighter Refractive Eye Surgery Program and Research Center, Fort Belvoir... Read More
Gender:
All
Ages:
22 years and above
Trial Updated:
04/14/2022
Locations: Navy Warfighter Refractive Surgery Center, San Diego, California
Conditions: Myopia, Astigmatism
Register for Updates