Clinical trials: Lenses
Cataract
Visual Performance of Bilateral AcrySof ReSTOR Aspheric +4
Determine the clinical visual outcomes following bilateral implantation of the AcrySof ReSTOR Aspheric Intraocular Lens (IOL) and to demonstrate what percentage of the subjects obtain spectacle freedom.
- Trial name
- NCT01215045
- Testing
- AcrySof ReSTOR Aspheric +4
- Where
- United States
- Volunteers
- 17 people, healthy volunteers welcome
- Sponsor
- Alcon Research
Cataract Senile
Prospective Evaluation of an Hydrophilic Acrylic Intraocular Lens
Evaluation of the clinical safety and effectiveness of an hydrophilic acrylic intraocular lens
- Trial name
- UVEA 809 (NCT04907500)
- Testing
- Intraocular lens
- Where
- Romania
- Volunteers
- 387 people
- Sponsor
- Carl Zeiss Meditec AG
Cataracts
A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens
Ambispective post-market data collection on visual symptoms, patient satisfaction and surgeon experience with the TECNIS PC IOL.
- Trial name
- NCT06250322
- Testing
- Intervention
- Where
- 20 sites in Australia, Austria and 6 more
- Volunteers
- 307 people
- Sponsor
- Johnson & Johnson Surgical Vision, Inc.
Aphakia, Postcataract, Cataract; Eye Disease
Safety and Efficacy of a Trifocal Intraocular Lens (IOL) POD L GF in Comparison With a Multifocal and a Monofocal IOL
The objectives of the Post-Market Follow-up (PMCF) clinical investigation are to determine the safety and performance of a hydrophobic trifocal intraocular lens POD L GF in comparison with two comparator lenses: another…
- Trial name
- NCT04005651
- Testing
- POD L GF IOL, Symfony® IOL, AcrySof® IOL
- Where
- 5 sites in France, Germany and 1 more
- Volunteers
- 100 people
- Sponsor
- Beaver-Visitec International, Inc.
Contact Lens Wear
A Safety and Effectiveness Study of BL-ABT12 Multi-Purpose Solution for Use by Participants With Soft Contact Lenses
This study is to evaluate the safety and effectiveness of ABT12 Multi-Purpose solution (Test) compared to COMPLETE® Multi-Purpose Solution Easy Rub® Formula ("COMPLETE Multi-Purpose Solution") when used by participants who are…
- Trial name
- NCT03897751
- Testing
- ABT12 Multi-Purpose Solution, COMPLETE Multi-Purpose Solution, Sensitive Eyes® Rewetting Drops
- Where
- 17 sites in United States
- Volunteers
- 252 people
- Sponsor
- Bausch & Lomb Incorporated
Astigmatism
Clinical Comparison of Two Silicone Hydrogel Toric Lenses in the US
The purpose of this trial is to compare the performance of two different contact lenses for contact lens wearers with astigmatism.
- Trial name
- NCT01007812
- Testing
- Lotrafilcon B contact lens, Comfilcon A contact lens
- Volunteers
- 50 people
- Sponsor
- CIBA VISION
Cataract
Intra-Operative Metrics With CENTURION® and INFINITI® Vision Systems
The purpose of this study is to evaluate intra-operative phacoemulsification machine metrics after phacoemulsification with the CENTURION® vision system configuration compared with the INFINITI® vision system configuration.
- Trial name
- NCT01848288
- Testing
- CENTURION® Vision System (CVS), INFINITI® Vision System (IVS)
- Volunteers
- 112 people
- Sponsor
- Alcon Research
Cataract
Long-term (3 Months) Safety of Femtosecond-laser Assisted Cataract Surgery
This clinical study is a prospective, post-market-clinical-follow-up study to investigate the long-term (3 months) safety of femtosecond laser assisted cataract surgery as a study follow-up extension to the Study #1304 titled as…
- Trial name
- NCT02023437
- Testing
- Femtosecond laser cataract surgery, Manual cataract surgery
- Where
- 2 sites in Czechia, India
- Volunteers
- 132 people
- Sponsor
- Technolas Perfect Vision GmbH
Contact Lens Wettability
Effect of FID 114675A on Lens Wettability
The purpose of this study is to evaluate lens wettability of contact lenses when used with an investigational multi-purpose disinfecting solution.
- Trial name
- NCT01342107
- Testing
- FID 114675A multi-purpose disinfecting solution (MPDS), Soft contact lens, Blister pack solution
- Where
- United States
- Volunteers
- 66 people
- Sponsor
- Alcon Research
Myopia
Non-Dispensing Evaluation of an Investigational Galyfilcon A Soft Contact Lens
The purpose of this investigation is to compare the fit characteristics and vision attributes of an investigational Galyfilcon A contact lens and an approved Galyfilcon A contact lens.
- Trial name
- NCT01054807
- Testing
- Galyfilcon A Habitual Lens, Galyfilcon A 8.7 BC (Investigational), Galyfilcon A 8.3 BC (Investigational)
- Where
- Australia
- Volunteers
- 32 people
- Sponsor
- Johnson & Johnson Vision Care, Inc.
Vision Correction
A Non-dispensing Fit Evaluation of Investigational Limbal Ring Soft Contact Lenses With Polyvinylpyrrolidone (PVP) in Asian Eyes
The purpose of this clinical trial is to compare the overall lens fit acceptance of two different soft contact lenses in an Asian population.
- Trial name
- NCT02036320
- Testing
- etafilcon A
- Where
- 7 sites in United States, Canada
- Volunteers
- 190 people, healthy volunteers welcome
- Sponsor
- Johnson & Johnson Vision Care, Inc.
Myopia
Ophthalmic Compatibility During Seven Days of Continuous Wear of Silicone Hydrogel Lenses
The purpose of this study is to assess the ophthalmic compatibility of three different silicone hydrogel lenses worn on an overnight basis for six nights.
- Trial name
- QUINCE (NCT00934102)
- Testing
- Narafilcon A contact lens, Lotrafilcon A contact lens, Galyfilcon A contact lens
- Where
- Canada
- Volunteers
- 57 people
- Sponsor
- CIBA VISION
Refractive Error, Myopia
Silicone Hydrogel Contact Lenses on Low Astigmatism in Japan
This study seeks to evaluate the clinical performance of a recently released contact lens designed to correct astigmatism to an established contact lens that has historically been used in these patients.
- Conditions
- Refractive Error, Myopia, Astigmatism
- Trial name
- NCT00639353
- Testing
- senofilcon A toric soft contact lens, senofilcon A sphere soft contact lens
- Where
- 10 sites in Japan
- Volunteers
- 102 people
- Sponsor
- Johnson & Johnson Vision Care, Inc.
Visual Acuity
Changes in Inflammatory Biomarkers When Symptomatic Contact Lens Wearers Are Refit in Acuvue Oasys 1-Day Lenses
This is a 5-Visit, single-arm, single-site, subject masked, dispensing trial to evaluate contact lens discomfort and inflammatory biomarker expression.
- Trial name
- NCT05120128
- Testing
- Acuvue® Oasys 1-Day
- Where
- United Kingdom
- Volunteers
- 34 people, healthy volunteers welcome
- Sponsor
- Johnson & Johnson Vision Care, Inc.
Myopia
Daytime Corneal Swelling During Wear of Narafilcon B Lenses
The purpose of this research is to measure daytime open-eye response to wearing of narafilcon B lenses.
- Trial name
- NCT01444287
- Testing
- narafilcon B, Polymacon, Lotrafilcon A
- Where
- Australia
- Volunteers
- 22 people
- Sponsor
- Johnson & Johnson Vision Care, Inc.
Visual Acuity
Evaluation of a Daily Disposable Novel Multifocal Contact Lens in a Myopic Population; Part 2
This is a 6-visit, subject-masked, multi-site, 2×3 crossover dispensing trial that will last approximately 2 - 4 months.
- Trial name
- NCT04615507
- Testing
- JJVC Investigational Multifocal Contact Lens, Dailies Total 1® Multifocal Contact Lens
- Where
- 6 sites in United States
- Volunteers
- 71 people, healthy volunteers welcome
- Sponsor
- Johnson & Johnson Vision Care, Inc.
Aphakia
Evaluation of the FluidVision Accommodating Intraocular Lens (AIOL) With an Improved Injector System
The purpose of this study is to evaluate the clinical outcomes of an investigational IOL in patients undergoing cataract extraction and intraocular lens implantation using an improved injector system.
- Trial name
- NCT02418871
- Testing
- FluidVision AIOL, Cataract surgery
- Where
- 5 sites in Hungary, South Africa
- Volunteers
- 53 people
- Sponsor
- PowerVision
Patients Who Have Bilateral NanoFlex Implantation at Least 3 Months Previously
Evaluation of Visual Outcomes of Monovision Patients Bilaterally Implanted With Nanoflex Intraocular Lenses
The purpose of this study is to look at how well you see the Nanoflex Intraocular lens placed in your eye.
- Trial name
- NCT01279122
- Testing
- Nanoflex IOL
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Innovative Medical
Visual Disorder
A Clinical Trial to Evaluate Investigational Silicone Hydrogel Contact Lenses Worn Continuously for One Week
This study is a prospective, randomized, double-masked, bilateral, dispensing, parallel-group clinical trial design. All subjects will participate in a 2-week daily disposable contact lens adaptation period prior to being…
- Trial name
- NCT02543528
- Testing
- Investigational Lens 1, Investigational Lens 2, Investigational Lens 3
- Where
- India
- Volunteers
- 171 people, healthy volunteers welcome
- Sponsor
- Johnson & Johnson Vision Care, Inc.
Correction of Refraction Error, Attenuation of Bright Light
Contact Lenses With New UV-blocker Manufactured With Different Techniques
This study is a randomized, 4-visit, double-masked, 2x3 bilateral crossover, dispensing trial. The study lenses will be worn as daily wear (DW) for a period of two weeks each with one of the study lenses being worn twice.
- Trial name
- NCT03475875
- Testing
- senofilcon A TEST Lens, senofilcon A CONTROL Lens
- Where
- 5 sites in United States
- Volunteers
- 92 people, healthy volunteers welcome
- Sponsor
- Johnson & Johnson Vision Care, Inc.
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