Alcon: all 719 studies
Page 5 of 8. Open to participants first (9), then studies with results posted, then the rest; newest registration first within each.
- Low Cylinder ToricCompletedNCT00732030Phase 4Results posted
- Contralateral ReSTOR / Monofocal or Phakic EyeCompletedNCT00731640Phase 4Results posted
- Evaluation of Deposits on Contact Lenses Worn Extended WearCompletedNCT00725530Not applicableResults posted
- Evaluation of Deposits on Contact Lenses Worn Daily WearCompletedNCT00725153Not applicableResults posted
- Visual Outcomes of Subjects Bilaterally Implanted With ReSTOR Aspheric +4 vs. Tecnis or Acri.LISACompletedNCT00721253Phase 4Results posted
- Visual Function After Implantation of Bilateral AcrySof ReSTOR Aspheric +3CompletedNCT00719732Phase 4Results posted
- DisCoVisc Versus DuoVisc, Healon5 and AmVisc PlusCompletedNCT00712244Phase 4Results posted
- Intraoperative Floppy Iris SyndromeCompletedNCT00711347Phase 4Results posted
- Blue Light Intraocular Lenses (IOLs) and PhotostressCompletedNCT00710996Results posted
- Visual Function With Bilateral AcrySof® ReSTOR® Aspheric SN6AD1CompletedNCT00710931Phase 4Results posted
- Visual Function With Contralateral AcrySof® ReSTOR® Aspheric SN6AD1 and SN6AD3TerminatedNCT00710905Phase 4Results posted
- Effects of Travatan Z and Xalatan on Ocular Surface HealthCompletedNCT00708422Phase 4Results posted
- Evaluation of SYSTANE Ultra Lubricant Eye DropsCompletedNCT00702377Not applicableResults posted
- Tobramycin Tear ConcentrationsCompletedNCT00695435Phase 1Results posted
- Comparison of Olopatadine 0.6% and Fluticasone Proprionate 50mcg Nasal Sprays in a Two Week Seasonal Allergic Rhinitis TrialCompletedNCT00691665Phase 4Results posted
- Travatan Z in Ocular Surface Health in Patients With Open-Angle Glaucoma or Ocular HypertensionCompletedNCT00690794Phase 3Results posted
- ACRYSOF® ReSTOR® Aspheric +3.0 D Add Power Intraocular Lens (IOL)CompletedNCT00684138Phase 4Results posted
- Acute Comfort of Lubricant Eye Drop FID 111421CompletedNCT00673959Not applicableResults posted
- Acute Comfort of Lubricant Eye Drops FID 112903CompletedNCT00673855Not applicableResults posted
- The Effect of Systane Ultra Lubricant Eye Drops (FID 112903) on Visual PerformanceCompletedNCT00673764Not applicableResults posted
- Assessment of Inflammatory Biomarkers Expressed in a Sjogren's Population: Effect of a Topical Steroid InterventionCompletedNCT00631358Phase 4Results posted
- Safety and Efficacy of Olopatadine HCl Nasal Spray in 6-11 Year Old PatientsCompletedNCT00578929Phase 3Results posted
- Safety Study of Olopatadine Nasal SprayCompletedNCT00578331Phase 3Results posted
- TOBRADEX Ophthalmic Suspension Versus Tobramycin 0.3%/Dexamethasone 0.05% Ophthalmic SuspensionCompletedNCT00576251Phase 3Results posted
- Acute Comfort and Blur of Systane and OptiveCompletedNCT00568386Not applicableResults posted
- A Single Dose Comfort Comparison of Travatan Z in One Eye Versus Xalatan in the Opposite Eye in Patients With Primary Open-Angle Glaucoma or Ocular HypertensionCompletedNCT00527592Phase 4Results posted
- Adherence Assessment With Travalert Dosing AidCompletedNCT00508469Phase 4Results posted
- A Phase IV Study of Travoprost + Brinzolamide to Treat Glaucoma or Ocular HypertensionCompletedNCT00471380Phase 4Results posted
- Study of Travatan and Cosopt in Primary Open-Angle Glaucoma or Ocular HypertensionTerminatedNCT00471068Phase 4Results posted
- Topical Treatment of Bacterial Conjunctivitis and Its Effect on Microbial FloraCompletedNCT00312338Phase 4Results posted
- A Long-term Safety Study of Once-daily TravatanCompletedNCT00051168Phase 3Results posted
- Evaluation of Tears Naturale® Free and Tears Naturale® II Lubricant Eye DropsCompletedNCT07540884Not applicable
- Contralateral Claims Study of Clareon Vivity ProActive, not recruitingNCT07484191Not applicable
- An Evaluation of the Safety and Tolerability of Ocular LubricantsCompletedNCT07238699Not applicable
- Post Market Clinical Evaluation of Clareon PanOptix Pro and Clareon PanOptix Pro Toric IOLsCompletedNCT07161635Not applicable
- Feasibility Study of an Accommodating IOL DesignActive, not recruitingNCT07147192Not applicable
- Reformulated PG324 Ophthalmic Solution for Intraocular Pressure ReductionCompletedNCT07082816Phase 3
- UNITY VCS Vitreoretinal SurgeryWithdrawnNCT07054281Not applicable
- A Cataract Surgery Clinical TrialWithdrawnNCT07044674Not applicable
- Clinical Investigation of a Femtosecond Laser for Corneal Flap CreationCompletedNCT07036835Not applicable
- OPTI-FREE Family STUDYWithdrawnNCT06592521Not applicable
- AOSEPT (CLEAR CARE) PLUS StudyWithdrawnNCT06588400Not applicable
- Evaluation of the Safety and Tolerability of Ocular LubricantsTerminatedNCT06571656Not applicable
- Evaluation of Reflex Tear ProductionTerminatedNCT06565624Not applicable
- Evaluation of AcrySof IQ Vivity Extended Vision Intraocular LensesWithdrawnNCT06541795Not applicable
- An Investigation of FID 123320 for the Reduction of Ocular Redness in Pediatric and Adult PopulationsCompletedNCT06538662Phase 3
- Cosmetic Contact Lenses Post-Market Clinical Follow-up StudyWithdrawnNCT06517316Not applicable
- Lotrafilcon B Plano Cosmetic Contact Lenses StudyWithdrawnNCT06493383Not applicable
- DAILIES TOTAL1® Soft Contact Lenses - Post-Market Clinical Follow-up StudyTerminatedNCT06483113
- Post-market Clinical Follow-up Study of Alcon PRECISION1™ Spherical and PRECISION1™ for Astigmatism Soft Contact LensesTerminatedNCT06462456
- A Double-Masked Comparison of FID 123320 Ophthalmic Solution to Vehicle for the Reduction of Ocular RednessCompletedNCT06444529Phase 3
- Next Generation RocklatanCompletedNCT06441643Phase 2
- Post-market Clinical Follow-up Study of Alcon TOTAL30® Contact Lenses (Lehfilcon A)TerminatedNCT06408649
- Clareon Toric Study (T2-T9)CompletedNCT06285695Not applicable
- EX-PRESS® P-50 and EX-PRESS® P-200CompletedNCT06119178
- Contralateral Study of WaveLight® Femtosecond Laser Devices for Corneal Flap CreationCompletedNCT06021353Not applicable
- Air Optix® Night and Day® Aqua Continuous WearCompletedNCT05992675
- Air Optix® Night and Day® Aqua Daily WearCompletedNCT05976750
- Air Optix® Night and Day® Aqua Therapeutic WearCompletedNCT05956535
- Systane® Hydration PF and Systane® Hydration PreservedCompletedNCT05932238Not applicable
- AONDA Therapeutic Indication Study ICompletedNCT05891106
- Evaluation of Safety and Tolerability of Investigational Ocular LubricantsCompletedNCT05888519Not applicable
- Air Optix Plus HydraGlyde Multifocal Daily/Extended Wear Contact LensesCompletedNCT05886894
- Air Optix Extended Wear Contact LensesCompletedNCT05886881
- Air Optix Daily Wear Contact LensesCompletedNCT05827224
- Clinical Comparison of Toric Contact Lenses Fit CharacteristicsWithdrawnNCT05805345Not applicable
- A Real-World Evidence (RWE) Long-Term Follow-Up Study to Assess Outcomes of Alcon Monofocal Intraocular LensesCompletedNCT05799950
- Clareon IOL Retrospective Data CollectionCompletedNCT05796674
- Post Market Clinical Follow-up (PMCF) Study of Clareon Vivity & Clareon PanOptixCompletedNCT05796453Not applicable
- Air Optix Night and Day Aqua (AONDA) Retrospective Study 1CompletedNCT05790928
- Study of AR-14034 in Participants With Neovascular Age-Related Macular Degeneration (nAMD)Active, not recruitingNCT05769153Phase 1/2
- Evaluation of Comfort of Ocular Lubricants in Symptomatic Contact Lens WearersCompletedNCT05741216Not applicable
- Evaluation of Safety and Tolerability of Ocular LubricantsCompletedNCT05573360Not applicable
- Study Evaluating Techniques for Measuring Tear ProductionCompletedNCT05497479Phase 1
- Post-Market Study of Alcon Intraocular LensesCompletedNCT05414565
- Clinical Study of a Fluid Accommodating Intraocular Lens (IOL) DesignActive, not recruitingNCT05317728Not applicable
- Safety and Effectiveness of the Hydrus MicrostentTerminatedNCT05198297Not applicable
- Systane Hydration in Subjects Undergoing Cataract SurgeryCompletedNCT05056233Not applicable
- Systane Complete Multi-symptom ReliefCompletedNCT05056155Not applicable
- Clinical Comparison of 2 Daily Disposable Toric Soft Contact LensesCompletedNCT05039112Not applicable
- Evaluation of Comfort in Symptomatic Contact Lens WearersCompletedNCT04963543Not applicable
- Evaluation of Comfort in Subjects With Moderate Dry Eye DiseaseCompletedNCT04830956Not applicable
- Real-World Study of Vivity Intraocular Lenses (IOLs)WithdrawnNCT04800016Not applicable
- Clinical Performance of a Daily Disposable Toric Silicone Hydrogel Contact LensCompletedNCT04464044Not applicable
- Exploratory Clinical Study for Techniques Associated With the Fluid Accommodating IOLCompletedNCT04330001Not applicable
- Clinical Performance Evaluation of Two Daily Disposable Silicone Hydrogel Toric Contact LensesCompletedNCT04254003Not applicable
- Clinical Performance of Two Daily Disposable Contact Lenses - Study 1CompletedNCT03969290Not applicable
- A Study Assessing AR-13503 Implant in Subjects With nAMD or DMECompletedNCT03835884Phase 1
- Post-Market Clinical Survey of Clareon® IOL AutonoMe™ in Japanese SubjectsCompletedNCT03824028
- India PanOptix Post Marketing StudyCompletedNCT03706066
- Study of Efficacy and Tolerability of SYSTANE Complete in Patients With Dry Eye DiseaseCompletedNCT03492541Not applicable
- Safety and Efficacy Study of the Hydrus Aqueous Implant in Subjects With POAGCompletedNCT03065036Phase 1/2
- Early Feasibility Study of UV-Femtosecond Laser Assisted Lenticular ExtractionCompletedNCT03021707Not applicable
- Cataract Surgery in Indian Patients With or Without LenSx® LaserWithdrawnNCT02605408
- A Controlled Study of the Aqueous Humor Dynamics of AR-13324 Ophthalmic Solution in Healthy Adult VolunteersCompletedNCT02406287Phase 1
- Safety Tolerability and Efficacy of Intravitreal LMG324 in the Treatment of Neovascular Age-Related Macular DegenerationTerminatedNCT02398500Phase 1/2
- A Real-World Registry to Investigate the Performance of LenSx® Laser in Chinese PatientsCompletedNCT02396719
- A Study of the Safety and Tolerability of Intravitreal LKA651 in Patients With Diabetic Macular EdemaWithdrawnNCT02281292Phase 1
- Study Assessing Ocular and Systemic Safety of AR-13324 in Healthy VolunteersCompletedNCT01997879Phase 1
- Multi-Center Clinical Evaluation of Two Daily Disposable Contact Lenses (Study 2)CompletedNCT01917162Not applicable