Alcon: all 719 studies

Page 2 of 8. Open to participants first (9), then studies with results posted, then the rest; newest registration first within each.

• Safety and Efficacy Study of PG324 (Netarsudil/Latanoprost 0.02% / 0.005%) Ophthalmic Solution Compared to GANFORT® Ophthalmic Solution in Open Angle Glaucoma or Ocular HypertensionCompletedNCT03284853Phase 3Results posted
• Clinical Investigation of AcrySof® IQ PanOptix™ IOL Model TFNT00CompletedNCT03280108Not applicableResults posted
• A Clinical Study of the ACRYSOF® IQ Extended Depth of Focus Intraocular Lens (IOL)CompletedNCT03274986Not applicableResults posted
• Post Approval Study of the CyPass SystemTerminatedNCT03273907Not applicableResults posted
• Clinical Investigation of the Visual Outcomes and Safety of a Trifocal Intraocular Lens (IOL) in a Korean PopulationCompletedNCT03268746Not applicableResults posted
• Hydrus Microstent for Refractory Open-Angle GlaucomaCompletedNCT03267134Not applicableResults posted
• Study of Netarsudil Ophthalmic Solution in Subjects With Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT)CompletedNCT03233308Phase 2Results posted
• Clinical Investigation of the Clareon® Intraocular Lens (IOL)CompletedNCT03170154Not applicableResults posted
• Clinical Comparison of Silicone Hydrogel Monthly LensesCompletedNCT03169153Not applicableResults posted
• Assessing Fitting Guides in Alcon Multifocal Contact LensesCompletedNCT03118934Not applicableResults posted
• Clinical Performance of a Silicone Hydrogel for Daily Disposable WearCompletedNCT03095027Not applicableResults posted
• Clinical Investigation of the AcrySof® IQ PanOptix™ IOLCompletedNCT03090256Not applicableResults posted
• Clinical Biocompatibility Evaluation of Contact Lens CoatingsCompletedNCT03034928Not applicableResults posted
• A Clinical Study of the ACRYSOF® IQ EDF Intraocular Lens (IOL)CompletedNCT03010254Not applicableResults posted
• Nocturnal/Diurnal Intraocular Pressure-Lowering Effect of Netarsudil Ophthalmic SolutionCompletedNCT02874846Phase 2Results posted
• Optimizing the Assessment of Refractive Outcomes After Cataract SurgeryCompletedNCT02842151Not applicableResults posted
• Clinical Investigation of Corneal Incision Size After Intraocular Lens (IOL) ImplantationCompletedNCT02826421Not applicableResults posted
• Clinical Outcomes Following Treatment With SYSTANE® BALANCECompletedNCT02776670Not applicableResults posted
• Clinical Evaluation of the Safety and Efficacy of FID 120947ACompletedNCT02771145Not applicableResults posted
• 24-hr Intraocular Pressure Control With SIMBRINZA ®CompletedNCT02770248Phase 4Results posted
• A Three Part Study of MGV354 in Ocular Hypertension or GlaucomaCompletedNCT02743780Phase 1/2Results posted
• Safety and Efficacy of SIMBRINZA® BID as an Adjunctive to DUOTRAV®TerminatedNCT02730871Phase 4Results posted
• Clinical Evaluation of DAILIES TOTAL 1® Performance in a Japanese PopulationCompletedNCT02710292Not applicableResults posted
• A Study to Assess Long-Term Safety of the CyPass Micro-Stent in Patients Completing the COMPASS TrialCompletedNCT02700984Not applicableResults posted
• Comparison of Lotrafilcon B Lenses With Different Packaging SolutionsCompletedNCT02699684Not applicableResults posted
• Clinical Evaluation of ACUVUE® OASYS® 1-Day and ACUVUE® OASYS®CompletedNCT02696317Not applicableResults posted
• Initial Performance of a Modified Daily Disposable Contact LensCompletedNCT02694835Not applicableResults posted
• Clinical Investigation of Visual Function After Bilateral Implantation of Two Presbyopia-Correcting Trifocal Intraocular Lenses (IOL)CompletedNCT02691741Not applicableResults posted
• Double-masked Study of PG324 Ophthalmic Solution in Patients With Open-angle Glaucoma or Ocular HypertensionCompletedNCT02674854Phase 3Results posted
• Accuracy of LASIK Flaps Created With the LenSx® Femtosecond Laser - A Pilot StudyCompletedNCT02575911Not applicableResults posted
• Double-masked Study of PG324 Ophthalmic Solution in Patients With Glaucoma or Ocular HypertensionCompletedNCT02558400Phase 3Results posted
• Double-masked Study of Netarsudil (AR-13324) Ophthalmic Solution in Subjects With Glaucoma or Ocular HypertensionCompletedNCT02558374Phase 3Results posted
• Pediatric Pharmacokinetic (PK) Study of EXE844 Otic Suspension in Otitis Media at the Time of Tympanostomy Tube Insertion (OMTT)CompletedNCT02539654Phase 1Results posted
• Investigation of AcrySof® IQ PanOptix™ Presbyopia-Correcting Intraocular Lens (IOL) Model TFNT00CompletedNCT02529488Not applicableResults posted
• DAILIES TOTAL1® - Comparative Assessment of Tear Film EvaporationCompletedNCT02517567Not applicableResults posted
• CLG561 Proof-of-Concept Study as a Monotherapy and in Combination With LFG316 in Subjects With Geographic Atrophy (GA)CompletedNCT02515942Phase 2Results posted
• Clinical Evaluation of Systane® Balance in Dry Eye SubjectsTerminatedNCT02511379Not applicableResults posted
• Safety and Pharmacokinetics of RTH258 in Subjects With Age-Related Macular DegenerationCompletedNCT02507388Phase 2Results posted
• Comparison of Centurion® Vision System With Balanced Tip and the Infiniti® Vision System With the Mini Flared Kelman (MFK) Tip During Cataract Extraction Surgery of Hard LensesCompletedNCT02502526Not applicableResults posted
• Comparison of Two Marketed Silicone Hydrogel LensesCompletedNCT02495948Not applicableResults posted
• Proof of Concept Study to Evaluate Safety and Efficacy of LME636 in the Treatment of Acute Anterior UveitisCompletedNCT02482129Phase 2Results posted
• Clinical Comparison of 27+® and 23-gauge ULTRAVIT® 7500 Cpm Vitrectomy OutcomesCompletedNCT02477605Not applicableResults posted
• Evaluation of Clinical Outcomes After the Use of SYSTANE® HYDRATIONCompletedNCT02470429Not applicableResults posted
• Clinical Evaluation Following Use of SYSTANE® ULTRA in the Management of Dry EyeCompletedNCT02446015Not applicableResults posted
• Safety and Efficacy of EXE844 Otic Suspension in Otitis Media at Time of Tympanostomy Tube Insertion (OMTT) - Study 2CompletedNCT02436304Phase 3Results posted
• Efficacy and Safety of RTH258 Versus Aflibercept - Study 2CompletedNCT02434328Phase 3Results posted
• Safety and Efficacy of EXE844 Otic Suspension in Otitis Media at Time of Tympanostomy Tube Insertion (OMTT)CompletedNCT02432105Phase 3Results posted
• SIMBRINZA® Suspension BID as an Adjunctive to Prostaglandin Analogue (PGA)CompletedNCT02419508Phase 4Results posted
• Clear Care® Plus vs. PeroxiClear™CompletedNCT02413333Not applicableResults posted
• DAILIES® AquaComfort Plus® Multifocal (MF) - Comparative Assessment of Visual PerformanceCompletedNCT02403180Not applicableResults posted
• Lubricity Post-Wear - Competitive Lenses PilotCompletedNCT02402127Not applicableResults posted
• Clinical Evaluation of MyDay™ and 1-DAY ACUVUE® TruEye®CompletedNCT02388763Not applicableResults posted
• A Clinical Study of Systane® Lid Wipes in BrazilCompletedNCT02380261Not applicableResults posted
• Clinical Evaluation of Systane® Gel Drops in Dry Eye SubjectsCompletedNCT02380248Not applicableResults posted
• Efficacy and Safety of Brinzolamide/Brimonidine Fixed Combination BID Compared to Brinzolamide BID Plus Brimonidine BID in Subjects With Open-Angle Glaucoma (OAG) or Ocular Hypertension (OHT)CompletedNCT02339584Phase 3Results posted
• Ocriplasmin for Vitreomacular Traction/Symptomatic Vitreomacular AdhesionCompletedNCT02322229Phase 4Results posted
• Olopatadine Hydrochloride Ophthalmic Solution Study in Chinese SubjectsCompletedNCT02322216Phase 3Results posted
• Efficacy and Safety of RTH258 Versus Aflibercept - Study 1CompletedNCT02307682Phase 3Results posted
• Formula Identification (FID) 114657 in Contact Lens WearersCompletedNCT02293538Not applicableResults posted
• Tear Film Evaluation of Dailies® AquaComfort Plus® Multifocal and ToricCompletedNCT02289742Not applicableResults posted
• DAILIES TOTAL1® Lens Centration in a Japanese PopulationCompletedNCT02252133Not applicableResults posted
• Effectiveness of Olopatadine HCl Ophthalmic Solution for the Treatment of Allergic Conjunctivitis in JapanCompletedNCT02251613Phase 4Results posted
• Clinical Evaluation of Opti-Free III (FID 109182) Compared to Opti-Free Plus® in JapanCompletedNCT02251561Not applicableResults posted
• Alcon® Ex-PRESS® Glaucoma Filtration Device in Japanese PatientsCompletedNCT02246777Not applicableResults posted
• Study of Netarsudil (AR-13324) Ophthalmic Solution in Patients With Glaucoma or Ocular HypertensionCompletedNCT02246764Phase 3Results posted
• DAILIES® AquaComfort Plus® Multifocal (MF) - Comparative Assessment of Visual PerformanceCompletedNCT02235831Not applicableResults posted
• Functional Vision With ACRYSOF® IQ IOLs Blue Light FiltrationCompletedNCT02219997Not applicableResults posted
• Evaluation of Netarsudil (AR-13324) Ophthalmic Solution in Patients With Glaucoma and Ocular HypertensionCompletedNCT02207621Phase 3Results posted
• Double-masked Study of AR-13324 Ophthalmic Solution in Patients With Glaucoma or Ocular HypertensionCompletedNCT02207491Phase 3Results posted
• Driving Simulator Study Comparing Two Modes of Presbyopic Correction With Contact LensesCompletedNCT02189863Not applicableResults posted
• Retrospective / Prospective Clinical Study of AcrySof® IQ ReSTOR® +2.5 D Multifocal Toric Intraocular LensesCompletedNCT02176343Not applicableResults posted
• A Comparison of Two Color Contact Lenses in Habitual Clear Contact Lens WearersCompletedNCT02175199Not applicableResults posted
• DW Evaluation of Lotrafilcon B Lenses in a Modified DesignCompletedNCT02157909Not applicableResults posted
• 6-Week Proof-of-Concept Study of Travoprost/Brinzolamide Ophthalmic Suspension in Subjects With Open-Angle Glaucoma or Ocular HypertensionCompletedNCT02140060Phase 2Results posted
• Multifocal High ADD Contact Lens Proof of Concept TrialCompletedNCT02117544Not applicableResults posted
• Comparative Evaluation of Contact Lens Centering of DAILIES® AquaComfort Plus® Versus 1-DAY ACUVUE® MOIST® in JapanCompletedNCT02103309Not applicableResults posted
• On-Eye Evaluation of Contact Lens Axis LocationCompletedNCT02100410Not applicableResults posted
• Tear Film Stability of DAILIES® AquaComfort Plus® Contact Lenses vs. MyDay® Daily Disposable Contact LensesCompletedNCT02089191Not applicableResults posted
• Safety and Efficacy Study of AL-53817 and AL-78843 Ophthalmic Solutions for Allergic ConjunctivitisCompletedNCT02079649Phase 2Results posted
• First-in-Human Study of LHA510 in Elderly Subjects and Patients With Age-Related Macular DegenerationCompletedNCT02076919Phase 1Results posted
• DAILIES TOTAL1® Lubricity Post WearCompletedNCT02072980Not applicableResults posted
• Visual Assessment of DAILIES® AquaComfort Plus® for Astigmatism as Compared to 1-DAY ACUVUE® MOIST® for AstigmatismCompletedNCT02071771Not applicableResults posted
• A Comparative Study of Two Daily Disposable Contact Lenses in Higher Myopia SubjectsCompletedNCT02066922Not applicableResults posted
• Study Assessing Safety and Efficacy of PG324 Ophthalmic Solution in Patients With Elevated Intraocular PressureCompletedNCT02057575Phase 2Results posted
• On-Eye Evaluation of Contact Lens Rotation MarksCompletedNCT02055404Not applicableResults posted
• Assessment of Patients Treated With JETREA® for Vitreomacular TractionCompletedNCT02035748Phase 4Results posted
• Comparing Hydrus Microstent(TM) to the iStent for Lowering IOP in Glaucoma Patients Undergoing Cataract SurgeryCompletedNCT02024464Not applicableResults posted
• Comparing Effectiveness of the Hydrus Microstent (TM) to Two iStents to Lower IOP in Phakic EyesCompletedNCT02023242Not applicableResults posted
• Efficacy of Travoprost/Timolol for Uncontrolled Intraocular PressureCompletedNCT02003391Phase 4Results posted
• Multifocal Lens Design EvaluationCompletedNCT01997216Not applicableResults posted
• Effectiveness of a Marketed One-Step Peroxide Lens Care Solution in Symptomatic Contact Lens WearersCompletedNCT01996709Not applicableResults posted
• Investigation of Intraocular Pressure (IOP) Reduction Efficacy of Travoprost Ophthalmic Solution in Patients With Normal Tension GlaucomaCompletedNCT01995136Phase 4Results posted
• Evaluation of Intraocular Pressure Using Simbrinza™ in Patients With Open-Angle Glaucoma or Ocular HypertensionCompletedNCT01978600Phase 4Results posted
• Clinical Outcomes Following Treatment With Systane® Balance in Dry Eye SubjectsCompletedNCT01967147Not applicableResults posted
• Evaluation of a New Daily Disposable Multifocal Contact Lens DesignCompletedNCT01951573Not applicableResults posted
• WaveLight® Refractive Myopic StudyCompletedNCT01941498Not applicableResults posted
• WaveLight® Refractive Flap Accuracy StudyCompletedNCT01941485Not applicableResults posted
• Effect of Blue Light Filtration on Visual PerformanceCompletedNCT01938989Not applicableResults posted
• Effect of SIMBRINZA® Suspension as an Added Therapy to a Prostaglandin AnalogueCompletedNCT01937312Phase 4Results posted
• Effect of SIMBRINZA® Suspension as an Added Therapy to TRAVATAN Z®CompletedNCT01937299Phase 4Results posted

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