Clinical trials: Error, Refractive
Eye Diseases, Presbyopia
Plasma Pharmacokinetics and Safety of LNZ101 and LNZ100 Ophthalmic Solutions in Healthy Adult Subjects With Presbyopia
This is a single-center, open-label, randomized study to assess the plasma pharmacokinetic profile of LNZ101 and LNZ100.
- Conditions
- Eye Diseases, Presbyopia, Refractive Errors, Brimonidine Tartrate
- Trial name
- NCT05936489
- Testing
- Aceclidine + Brimonidine, Aceclidine
- Where
- United States
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- LENZ Therapeutics, Inc
Myopia, Astigmatism
A Study to Evaluate the Safety and Effectiveness of the 217z Laser With Zyoptix for Lasik
A Study to demonstrate the safety and efficacy of wavefront laser refractive surgery treatments for myopia and astigmatism.
- Trial name
- NCT00347997
- Testing
- 217z Laser
- Volunteers
- healthy volunteers welcome
- Sponsor
- Bausch & Lomb Incorporated
Refractive Error
Comparison of Anterior Corneal Optical Aberration Induced by CK and Hyperopic LASIK
Conductive keratoplasty (CK) had shown to be a safe and effective procedure for the treatment of low to moderate hypeopia. It had been approved by the U.S. Food and Drug Administration (FDA) to treat presbyope in early 2004.
- Trial name
- NCT04676620
- Testing
- CK surgery
- Where
- China
- Volunteers
- 69 people
- Sponsor
- Wang Hongxia
Astigmatism
Non-dispensing Study to Check Prescription Equivalence of Two Daily Disposable Toric Contact Lens Types
The purpose of this study is to determine whether the prescription determined for a new daily disposable toric contact lens will be a good match to a prescription determined for an existing brand of lens.
- Trial name
- NCT01120782
- Testing
- etafilcon A toric contact lens with new wetting agent, etafilcon A toric contact lens
- Where
- 2 sites in United States
- Volunteers
- 45 people
- Sponsor
- Johnson & Johnson Vision Care, Inc.
Hyperopic Astigmatism
Effect of WRAD Lens on Axial Growth and Refraction in Low-hyperopic Chinese Children
Myopia is one of the most common visual impairments worldwide.This not only poses long-term risks to individual health but also imposes significant medical and economic burdens on society.
- Trial name
- NCT07682974
- Testing
- With-the-Rule Astigmatic Defocus Lens, With-the-Rule Astigmatic Defocus Lens (Non-plano), Single Vision
- Volunteers
- 117 people, healthy volunteers welcome
- Sponsor
- He Eye Hospital
Myopia
Study of Safety and Effectiveness of the Boston Orthokeratology Shaping Lens in the Arise Orthokeratology Lens
The objective of this orthokeratology study is to evaluate the safety and effectiveness of the Arise Orthokeratology Lens with non-spherical posterior peripheral curves
- Trial name
- NCT05984290
- Testing
- orthokeratology lens
- Where
- 6 sites in United States
- Volunteers
- 90 people
- Sponsor
- Bausch & Lomb Incorporated
Refractive Surgery
Topography Guided LASIK by Different Protocols for Treatment of Astigmatism
Background and Rationale: LASIK has been among the highest satisfaction rates of surgical procedures, ranging from 82%-98%. Different ablation profiles have been developed over the years.
- Trial name
- NCT03597906
- Testing
- topography guided ablation, manifest refraction, full topography modified refraction
- Where
- Egypt
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Cairo University
Refractive Errors
Comparison of Higher Order Aberrations and Contrast Sensitivity Between Acrysof SN60AT, SN60WF and Restore Intraocular Lenses
This project involves evaluation of post operative contrast sensitivity and wavefront aberration results among patients implanted with standard monofocal lenses (Acrysof SN60AT/SN60WF) and the new presbyopic correcting multifocal…
- Trial name
- NCT00345085
- Testing
- Wavefront and Contrast Sensitivity
- Where
- United States
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- University of Texas Southwestern Medical Center
Myopia, Astigmatism
Early Changes Between Lenticule Extraction and Small-Incision Lenticule Extraction
The aim is to evaluate the short-term changes in ocular surface measures and tear inflammatory mediators after lenticule extraction (FLEx) and small-incision lenticule extraction (SMILE) procedures.
- Trial name
- NCT02540785
- Testing
- lenticule extraction, small-incision lenticule extraction
- Volunteers
- 41 people, healthy volunteers welcome
- Sponsor
- Sun Yat-sen University
Myopia
Efficacy of LASIK Versus PRK in Asians With Mild and Moderate Myopia
Laser in situ keratomileusis (LASIK) and photorefractive keratectomy (PRK) are currently the 2 main refractive surgeries to correct myopia which are being performed worldwide, with more patients preferring LASIK to PRK because of…
- Trial name
- NCT00348049
- Testing
- Laser in Situ Keratomileusis (LASIK), Photorefractive Keratectomy (PRK)
- Where
- Singapore
- Sponsor
- Singapore National Eye Centre
Myopia
A Prospective Evaluation of Contrast Sensitivity and Disability Glare in Refractive Surgery, a Sub-Study of: Initial Evaluation of Excimer Laser Keratorefractive Surgery in U.S. Army Personnel (WU # 2335-99)
The purpose of this study is to conduct a prospective assessment of small target contrast sensitivity and disability glare in refractive surgery.
- Trial name
- NCT00413868
- Testing
- LASIK, PRK, Small target contrast sensitivity and disability glare
- Where
- United States
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Walter Reed Army Medical Center
Hyperopia, Farsightedness
The Emmetropization Via Accommodation (EVA) - II Study
To determine if wearing a novel treatment during a 15-month period will enhance emmetropization in 4-month-old infants who have demonstrated poor ocular accommodation (eye focusing).
- Conditions
- Hyperopia, Farsightedness, Hypermetropia
- Trial name
- EVA-II (NCT07838597)
- Testing
- Experimental treatment arm
- Where
- United States
- Volunteers
- 52 people
- Sponsor
- Ohio State University
Myopia, Astigmatism
LASIK Surgery With a New Laser for the Treatment of Myopia Without Astigmatism
The AQUARIUZ ablation laser is a solid-state laser and has been CE approved for corneal surgery since March 2020 for the treatment of short- and longsightedness with and without astigmatism.
- Trial name
- AQUARIUZ2020 (NCT04794023)
- Testing
- Corneal Ablation
- Where
- Switzerland
- Volunteers
- 27 people
- Sponsor
- Ziemer Ophthalmic Systems AG
Myopia
Intravitreal Bevacizumab and Low Fluence Photodynamic Therapy
The purpose of this study is to report the treatment effect and safety of combined intravitreal bevacizumab (IVB) and photodynamic therapy (PDT) with verteporfin using a reduced (RF) light fluence rate, in choroidal…
- Trial name
- NCT00802126
- Testing
- Combination therapy "IVB + rf-PDT"
- Where
- Italy
- Volunteers
- 16 people
- Sponsor
- University of Campania Luigi Vanvitelli
Astigmatism
Clinical Evaluation of Toric Intraocular Lens Made by Aurolab
The purpose of this study is to measure visual acuity and Intraocular Lens (IOL) rotational stability after implantation of TORIC IOL and to assess the post operative complications after implantation of TORIC IOL.
- Trial name
- TORICIOL (NCT01396616)
- Testing
- Experimental - Toric Intraocular lenses
- Where
- India
- Volunteers
- 120 people
- Sponsor
- Aurolab
Retinal Diseases, Choroidal Disease
An Interpretable Fundus Diseases Report Generating System Based On Weakly Labelings
To establish a multimodal fundus image report generation model to realize an interpretable system for multiple fundus diseases, multimodal image analysis, diagnosis, and treatment decision automatic reporting based on weakly…
- Conditions
- Retinal Diseases, Choroidal Disease, Pathological Myopia, Diabetic Retinopathy
- Trial name
- NCT06918028
- Testing
- With fundus diseases, Without fundus diseases
- Where
- China
- Volunteers
- 9,999 people, healthy volunteers welcome
- Sponsor
- Zhongshan Ophthalmic Center, Sun Yat-sen University
Refractive Errors
Study to Evaluate the Safety and Efficacy of HI-BRITE Large Diameter Rigid Gas Permeable Contact Lens
Study to evaluate the safety and efficacy of HI-BRITE large diameter rigid gas permeable contact lens (hexafocon b) test when worn on a daily wear basis in the correction of myopia/hyperopia/astigmatism/presbyopia/ and irregular…
- Trial name
- NCT02812316
- Testing
- HI-BRITE Large Diameter Rigid Gas Permeable Contact Lens
- Where
- Taiwan
- Volunteers
- 136 people, healthy volunteers welcome
- Sponsor
- Taipei Medical University Hospital
Presbyopia, Refractive Errors
Safety and Efficacy of a Sub-epitheilal Transform™ Corneal Allograft (TCA) for Presbyopia Correction
The objective of this clinical study is to evaluate the safety and effectiveness of subepithelial implantation of the Allotex TransForm corneal allograft (TCA) for improving near vision in presbyopic subjects.
- Trial name
- NCT03675438
- Testing
- Sub-epitheilal TCA Inlay
- Where
- 11 sites in Austria, Belgium and 4 more
- Volunteers
- healthy volunteers welcome
- Sponsor
- Allotex, Inc.
Myopia
Investigation of the Clinical Performance of Silicone Hydrogel Contact Lenses During Continuous Wear
The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens during continuous wear (up to 30 nights) over a period of 24 months.
- Trial name
- NCT00346593
- Testing
- Silicone hydrogel contact lens
- Where
- Australia
- Sponsor
- University of Melbourne
Myopia, Myopia Progression
The P.A.U.S.E.® Spectacle Study
The goal of this clinical trial is to learn if spectacle lenses using Phase Alteration Utilising Sub Elements (P.A.U.S.E.®) technology works to slow down the rate of myopia progression in myopic children.
- Trial name
- NCT06577948
- Testing
- Single vision spectacle lens, P.A.U.S.E. spectacle lens 1, P.A.U.S.E. spectacle lens 2
- Where
- Vietnam
- Volunteers
- 205 people
- Sponsor
- nthalmic Pty Ltd
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