Clinical trials: Lenses
Myopia
Comparing The Performance Of Two Different Daily Disposable Lenses (MIKI)
The objective of the study is to evaluate and compare the performance of study test lens to study control lens, when worn on a daily disposable modality over a period of approximately one week each
- Trial name
- NCT04492397
- Testing
- Test Contact Lens, Control Contact Lens
- Where
- Canada
- Volunteers
- 35 people, healthy volunteers welcome
- Sponsor
- CooperVision, Inc.
Cataract
Study to Evaluate the Safety for the Treatment of Inflammation Associated With Cataract Surgery
The study is a prospective, randomized, parallel-design, multicenter trial in patients ≥40 years of age undergoing cataract surgery.
- Trial name
- NCT02547623
- Testing
- Dexamethasone, Prednisolone
- Where
- 11 sites in United States
- Volunteers
- 194 people
- Sponsor
- ICON Bioscience Inc
Myopia
Evaluation of The Comfort of Orthokeratology Lenses Fit Using A New Software
As new orthokeratology fitting software emerges onto the market, it is of interest to assess their usefulness in guiding eye practitioners with lens fit.
- Trial name
- NCT05389072
- Testing
- control contact lens
- Where
- 4 sites in United States, Spain
- Volunteers
- 57 people, healthy volunteers welcome
- Sponsor
- CooperVision International Limited (CVIL)
Myopia
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
- Trial name
- NCT01952665
- Testing
- comfilcon A, lotrafilcon B
- Where
- 6 sites in United States
- Volunteers
- 63 people
- Sponsor
- CooperVision, Inc.
Pars Plana Vitrectomy
Safety and Efficacy of HydroLenz for Vitrectomy-Induced Lens Opacities
The primary objective of this study is to provide safety data for two different dosages of HydroLenz. Secondary objectives are to provide preliminary data to determine whether HydroLenz has the same effect in humans as it does in…
- Trial name
- NCT05592912
- Testing
- HydroLenz Injection, No HydroLenz Injection
- Sponsor
- PromiSight, LLC
Astigmatism
Comparison of Two Silicone Hydrogel Toric Contact Lenses
The purpose of this research study is to compare the performance of two different types of Alcon soft toric study contact lenses to obtain information on study lens orientation.
- Trial name
- NCT03392532
- Testing
- Lotrafilcon B toric contact lenses with HYDRAGLYDE, Lotrafilcon B toric contact lenses
- Where
- United States
- Volunteers
- 36 people
- Sponsor
- Alcon Research
Contact Lens Solutions
Safety and Efficacy of a Bausch & Lomb Multipurpose Solution When Compared to Ciba Vision Aquify Multipurpose Solution
To the safety and efficacy of a Bausch \& Lomb Multipurpose Solution when compared to Ciba vision Aquify Multipurpose solution
- Trial name
- NCT00636363
- Testing
- Bausch & Lomb Multipurpose Solution - Rub Care, Bausch & Lomb Multipurpose Solution - No Rub Care, Ciba Vision Aquify Multipurpose Solution
- Where
- United States
- Volunteers
- 541 people
- Sponsor
- Bausch & Lomb Incorporated
Inflammation, Cataracts
The Efficacy and Safety of IBI-10090 for the Treatment of Inflammation Associated With Cataract Surgery
The purpose of this study is to determine whether IBI-10090 injection is effective in the treatment of inflammation associated with cataract surgery.
- Trial name
- NCT02006888
- Testing
- IBI-10090
- Where
- United States
- Volunteers
- 394 people
- Sponsor
- ICON Bioscience Inc
Ametropia
Clinical Evaluation of HPT Treated Rigid Contact Lenses Made From Hexafocon A
This will be an up to six months, subject-masked, contralateral, parallel-group, randomised, daily wear study. All subjects will wear the Test lens in one eye and the Control lens in the other eye.
- Trial name
- NCT04525170
- Testing
- HPT treatment, untreated
- Where
- 2 sites in Germany
- Volunteers
- healthy volunteers welcome
- Sponsor
- Contamac Ltd
Refractive Error, Glaucoma
A Post-market Clinical Study to Collect Safety and Performance Data on Johnson & Johnson Surgical Vision Products
Retrospective collection of data from medical records, multicenter, post-market clinical follow-up study.
- Conditions
- Refractive Error, Glaucoma, Cataracts, Clear Lens Exchange
- Trial name
- NCT05394324
- Testing
- Intervention
- Where
- 13 sites in United States, Germany and 1 more
- Volunteers
- 1,674 people
- Sponsor
- Johnson & Johnson Surgical Vision, Inc.
Contact Lens Complication
A Clinical Study Comparing the Comfort of Three Commercially Available Contact Lenses
The purpose of this study is to compare the comfort of three commercially available contact lenses.
- Trial name
- NCT02298400
- Testing
- Acuvue® Oasys® Lenses (senofilcon A), 30-Day Bausch + Lomb PureVision (balafilcon A), Clariti® 1-Day (Somofilcon A)
- Where
- United States
- Sponsor
- ORA, Inc.
Presbyopia, Refractive Errors
Assessing Fitting Guides in Alcon Multifocal Contact Lenses
The purpose of this study is to compare an alternative fitting guide to a current fitting guide for optimizing contact lens parameters and determining contact lens prescription.
- Trial name
- NCT03118934
- Testing
- Lotrafilcon B multifocal contact lenses, Nelfilcon A multifocal contact lenses, Delefilcon A multifocal contact lenses
- Where
- 20 sites in United States, Canada and 1 more
- Volunteers
- 188 people
- Sponsor
- Alcon Research
Myopia
Comparative Performance of PureVision Lens Designs
The objective of this study is to evaluate the performance of the PureVision Lens designs when worn on a 30-day continuous wear basis
- Trial name
- NCT00661687
- Testing
- Currently Marketed PureVision Contact Lens., Alternate Design of the PureVision Contact Lens.
- Where
- 2 sites in Malaysia, Philippines
- Volunteers
- 206 people
- Sponsor
- Bausch & Lomb Incorporated
Cataract, Presbyopia
IOL Implantation After KAMRA Inlay Removal
A. The primary purpose of the study is to evaluate outcomes of aphakic eyes implanted with the IC-8 IOL following cataract removal in prior inlay patients after KAMRA inlay removal. B.
- Trial name
- NCT03320473
- Testing
- IC-8 IOL
- Where
- Philippines
- Volunteers
- 29 people, healthy volunteers welcome
- Sponsor
- AcuFocus, Inc.
Cataract, Corneal Astigmatism
Post-market Study to Obtain Surgeon Feedback on Clinical Outcome in Eyes Implanted With TECNIS Toric II IOL
This is a multicenter, prospective, single-arm, open-label, clinical study of the commercially available TECNIS Toric II, Model ZCU IOL.
- Trial name
- NCT04210232
- Testing
- TECNIS® TORIC II Intraocular Lens (IOL)
- Where
- 12 sites in United States
- Volunteers
- 54 people
- Sponsor
- Johnson & Johnson Surgical Vision, Inc.
Myopia, Astigmatism
Evaluation of Orthokeratology Lenses With a 5MM Optic Zone Diameter
To evaluate the clinical performance and user-reported experience of Paragon CRT contact lenses with a 5mm Optic Zone Diameter (OZD)
- Trial name
- NCT07751172
- Testing
- Lens A (paflufocon D)
- Where
- 3 sites in United States, Spain
- Volunteers
- 70 people
- Sponsor
- CooperVision International Limited (CVIL)
Myopia
Comparison of Clinical Performance and Subjective Preference of Three Contact Lenses
The purpose of this study is to evaluate the clinical performance and subject's preference out of three LRE (Limbal Ring Enhancing) lens types: etafilcon A (Johnson\&Johnson), methafilcon A (Interozzo), and methafilcon A…
- Trial name
- NCT03134599
- Testing
- etafilcon A, methafilcon A - Interozzo, methafilcon A - CVI (CooperVision)
- Where
- South Korea
- Volunteers
- 60 people
- Sponsor
- CooperVision, Inc.
Refractive Errors
Clinical Assessment of Two Daily Wear Reusable Soft Silicone Hydrogel Contact Lenses
The overall objective of this clinical study is to describe the clinical performance of the TOTAL30® soft contact lens compared to the ACUVUE® OASYS® with HYDRACLEAR PLUS (AOHP) soft contact lens in a daily wear modality.
- Trial name
- NCT05056987
- Testing
- Lehfilcon A contact lenses, Senofilcon A contact lenses, AOSEPT PLUS with HydraGlyde
- Where
- United Kingdom
- Volunteers
- 36 people
- Sponsor
- Alcon Research
Corneal Deformity
Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens
This will be a randomized non-dispensing study comparing the overnight corneal swelling of an eye while wearing no contact lens to the Ultra contract lens.
- Trial name
- NCT02258139
- Testing
- B&L Investigational Contact Lens
- Where
- United States
- Volunteers
- 38 people, healthy volunteers welcome
- Sponsor
- Bausch & Lomb Incorporated
Cataract Senile
Extended Depth of Focus (EDF) Intraocular Lens (IOL) Versus Monofocal Intracoular Lens (IOL)
Extended depth of focus (EDF) intraocular lens (IOL) versus Monofocal intraocular lens (IOL)
- Trial name
- NCT07092020
- Testing
- EDF, Monofocal IOL
- Where
- 14 sites in Bulgaria, Czechia and 2 more
- Volunteers
- 220 people
- Sponsor
- Carl Zeiss Meditec AG
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