Clinical trials: Lens Disease
Cataract
ReSTOR Natural +3.0D Study In Japan
The objective of this study is to evaluate safety and effectiveness of ACRYSOF Multifocal Single-piece Intraocular Lens (IOL) Model SN6AD1 when implanted to replace the natural lens following cataract removal.
- Trial name
- NCT00758576
- Testing
- ACRYSOF Multifocal Single-piece Intraocular Lens (IOL) Model SN6AD1
- Where
- Japan
- Volunteers
- 64 people
- Sponsor
- Alcon Research
Myopia
Performance Evaluation of a New Daily Disposable Silicone Hydrogel Lens
The purpose of this study was to compare a new daily disposable, silicone hydrogel contact lens to marketed daily disposable, silicone hydrogel contact lenses.
- Trial name
- TUNGSTEN (NCT01371552)
- Testing
- delefilcon A contact lens, filcon II 3 contact lenses, narafilcon A contact lenses
- Where
- Canada
- Volunteers
- 119 people
- Sponsor
- CIBA VISION
Aphakia, Cataract
RxSight Light Adjustable Lens and Light Delivery Device New Enrollment Study
The primary objective of this study is to conduct a post-approval study which compares the LAL to a monofocal control IOL for safety outcomes.
- Trial name
- NCT05202808
- Testing
- Light Adjustable lens (LAL) and Light Delivery Device (LDD), Control IOL
- Where
- 14 sites in United States
- Volunteers
- 500 people
- Sponsor
- RxSight, Inc.
Cataract
Clareon TruPlus vs Tecnis Eyhance IOLs in Cataract Patients
This study is a prospective, randomized, two-arm, single-center, single-surgeon, double-masked (subject and assessor) comparative study.
- Trial name
- NCT07658040
- Testing
- Clareon TruPlus, Tecnis Eyhance
- Where
- United States
- Volunteers
- 70 people
- Sponsor
- Gainesville Eye Associates
Myopia
A Study to Evaluate the Product Feasibility of Two New Silicone Hydrogel Contact Lenses
The objective of this study is to determine the clinical feasibility and to evaluate the product performance of two RD2135-01 investigational soft contact lenses (Test 1 and Test 2) developed by Bausch + Lomb.
- Trial name
- NCT01583868
- Testing
- B&L RD2135-01 lens C, B&L RD2135-01 lens D, PureVision2
- Where
- United States
- Volunteers
- 216 people
- Sponsor
- Bausch & Lomb Incorporated
Myopia, Hyperopia
A Clinical Comparison of Two Soft Contact Lenses
The study objective was to gather short-term clinical performance data for two soft contact lenses.
- Trial name
- NCT05741450
- Testing
- Lens 1 (monthly replacement), Lens 2 (daily disposable)
- Where
- United Kingdom
- Volunteers
- 45 people
- Sponsor
- CooperVision, Inc.
Open Angle Glaucoma, Ocular Hypertension
Selective Laser Trabeculoplasty After Failed Phacoemulsification With Eximer Laser Trabeculectomy
The aim of this study is to evaluate the efficacy of selective laser trabeculoplasty after a prior failed phacoemulsification and Eximer Laser Trabeculectomy.
- Conditions
- Open Angle Glaucoma, Ocular Hypertension, Cataract
- Trial name
- SLT (NCT02434250)
- Testing
- Selective Laser Trabeculoplasty
- Where
- Switzerland
- Volunteers
- 203 people
- Sponsor
- University of Zurich
Dry Eye
A Study to Evaluate Concomitant Perfluorohexyloctane Use With Contact Lens Wear
Assess the impact of concomitant Miebo use while wearing contact lenses
- Trial name
- NCT07054606
- Testing
- Perfluorohexyloctane ophthalmic solution
- Where
- 6 sites in United States
- Volunteers
- 104 people
- Sponsor
- Bausch & Lomb Incorporated
Presbyopia
Clinical Efficacy of the Pinhole Soft Contact Lenses for Correcting Presbyopia
For correct of presbyopia, in this study, the investigators have recruited subjects who aged 45~65 years with presbyopia and do not have any other ocular disease(ex, ocular surface disease, corneal dystrophy, retinal disorders…
- Trial name
- NCT02612584
- Testing
- Pinhole Soft Contact Lens apply for presbyopia
- Where
- South Korea
- Volunteers
- 30 people
- Sponsor
- Yonsei University
Myopia
Myopia Control Using Novel Soft Contact Lenses
The goal of this study is to investigate the myopic control efficacy of two study soft contact lenses in children. Participants will be prescribed Lens A, Lens B or single vision contact lenses for the first year.
- Trial name
- NCT07547085
- Testing
- Lens A, Lens B
- Where
- Hong Kong
- Volunteers
- 126 people
- Sponsor
- The Hong Kong Polytechnic University
Cataract
Clinical Evaluation of the Next Generation Phaco System
This study is a prospective, open-label clinical study of the VERITAS Vision System. The study will be conducted at up to three sites, with minimum 55 eyes and up to 150 eyes to be treated.
- Trial name
- ALPINE (NCT04332640)
- Testing
- VERITAS Vision System
- Where
- 2 sites in United States, El Salvador
- Volunteers
- 79 people
- Sponsor
- Johnson & Johnson Surgical Vision, Inc.
Myopia Progression
Orthokeratology Lens Decentration with Two Designs of Corneal Refractive Therapy™ Lenses: a One-year Prospective Study
Background/Objectives: To examine the trend of treatment zone (TZ) decentration over 12 months of Orthokeratology (OK) wear using two corneal refractive therapy (CRT) lens designs: standard (STD) and dual axis (DA).
- Trial name
- NCT06726499
- Testing
- Spherical CRT, Toric CRT
- Where
- Spain
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- Universidad Complutense de Madrid
Myopia
An Evaluation of the Effectiveness of Dual Focus Soft Contact Lenses in Slowing Mypoia Progression
The purpose of this study is to determine whether a new type of soft contact lens with a unique optical design (dual focus) is effective at slowing the progression of myopia (near-sightedness) in children.
- Trial name
- NCT01729208
- Testing
- Dual Focus Soft Contact Lens, Single Vision Soft Contact Lens
- Where
- 4 sites in Canada, Portugal and 2 more
- Volunteers
- 144 people
- Sponsor
- CooperVision, Inc.
Myopia
Clinical Evaluation of Two Daily Wear Silicon Hydrogel Contact Lens
The purpose of this study is to demonstrate that the VISCO (Olifilcon A) soft contact lens could be prescribed as a supportive care for myopic persons.
- Trial name
- NCT02354924
- Testing
- Biofinity soft contact lens, Visco soft contact lens
- Volunteers
- 60 people
- Sponsor
- Visco Vision Inc.
Cataract, Pseudoexfoliation Syndrome
Long-term Intraocular Lens (IOL) Decentration and Tilt in Eyes With Pseudoexfoliation Syndrome (PES) Following Cataract Surgery
To evaluate long-term intraocular lens (IOL) decentration and tilt in eyes with pseudoexfoliation syndrome (PES) following cataract surgery using Visante anterior segment OCT and iTrace Visual Function Analyzer.
- Conditions
- Cataract, Pseudoexfoliation Syndrome, Pseudophakia
- Trial name
- NCT03453827
- Testing
- no intervention
- Volunteers
- 37 people
- Sponsor
- Hospital Hietzing
Lenses, Intraocular, Visual Fields
Visual Field Changes in TECNIS ZCB00 Monofocal vs. TECNIS Symfony Extended Depth of Focus Intraocular Lens Implantation
Glaucoma is a leading cause of blindness worldwide. Damage to the optic nerve results in vision loss gradually. This vision loss can be detected by using visual field testing, and is a way of monitoring glaucoma progression.
- Conditions
- Lenses, Intraocular, Visual Fields, Cataract
- Trial name
- NCT03505827
- Testing
- 24-2 SITA Standard Humphrey Visual Field Test
- Where
- 2 sites in Canada
- Sponsor
- Western University, Canada
Astigmatism, Myopia
Effect of a Myopia Control Lens on the Astigmatism in Children
The goal of this clinical trial is to investigate over a one-year period the effect of myopia control spectacle lenses on astigmatism in children aged 6 to 13 years with myopia and astigmatism.
- Trial name
- MAC (NCT07810725)
- Testing
- Lenslet-based myopia control spectacle lens
- Volunteers
- 15 people
- Sponsor
- Essilor International
Myopia
Controlling Myopia Progression With Soft Contact Lenses (Contact Lens Control)
This study is to investigate whether novel soft contact lens optical designs can slow myopia progression
- Trial name
- NCT01829191
- Testing
- Soft Contact Test Lens A, Soft Contact Test Lens C
- Where
- United States
- Volunteers
- 174 people, healthy volunteers welcome
- Sponsor
- Johnson & Johnson Vision Care, Inc.
Astigmatism, Far Sightedness
Clinical Results of a Monofocal Aspheric Bitoric Intraocular Lens With Plate Haptics in Hyperopic Eyes (HIPER-AT-TORBI)
Observational post-marketing study with prospective follow-up of CE marked medical devices aimed at the treatment of hyperopia and astigmatism in patients with cataract.
- Conditions
- Astigmatism, Far Sightedness, Cataracts
- Trial name
- HIPER-AT-TORBI (NCT05058274)
- Testing
- Implant of the AT-TORBI 709 lens
- Where
- 2 sites in Spain
- Volunteers
- 60 people
- Sponsor
- OFTALVIST (Oftalmología Vistahermosa S.L)
Myopia
Lens Fitting Evaluation of CooperVision MyDay™ Compared With 1-DAY ACUVUE® TruEye® and DAILIES TOTAL1®
Lens Fitting Evaluation of CooperVision MyDay™ Compared with 1-DAY ACUVUE® TruEye® and DAILIES TOTAL1®
- Trial name
- NCT02341859
- Testing
- stenfilcon A, delefilcon A, narafilcon A
- Where
- United States
- Volunteers
- 22 people
- Sponsor
- CooperVision, Inc.
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