Alcon: Dry Eye Syndromes trials
The registry lists 88 Dry Eye Syndromes studies with Alcon as lead sponsor. 1 are open to participants now and 37 have results posted.
Phase 1 2Phase 2 6Phase 3 8Phase 4 8No phase 64(a study in two phases counts in both)
Studies
Open to participants first, then studies with results posted, then the rest; newest registration first within each.
- UNITY DX Cornea StudyRecruitingNCT07768735
- A Study to Evaluate 0.003% AR-15512 Safety and Drop AttributesCompletedNCT06660290Phase 3Results posted
- A Study Designed to Evaluate Tear ProductionCompletedNCT06544707Phase 3Results posted
- A Study to Investigate the Effect of 0.003% AR-15512 on Subjects With Dry Eye DiseaseCompletedNCT06544694Phase 3Results posted
- Study of Safety and Performance of a Novel Ocular Lubricant in Subjects With Dry Eye DiseaseCompletedNCT06444516Not applicableResults posted
- Systane® Complete Preservative Free Lubricant Eye DropsCompletedNCT05932225Not applicableResults posted
- Systane® Ultra Preservative Free Lubricant Eye DropsCompletedNCT05902364Not applicableResults posted
- A Long-Term Safety Study Evaluating the Safety and Systemic Exposure of AR-15512CompletedNCT05493111Phase 3Results posted
- Study Evaluating the Safety and Efficacy of AR-15512 (COMET-3)CompletedNCT05360966Phase 3Results posted
- Study Evaluating the Safety and Efficacy of AR-15512CompletedNCT05285644Phase 3Results posted
- A Phase 2b Study Evaluating the Safety and Efficacy of AR-15512 Ophthalmic Solution for the Treatment of Dry Eye DiseaseCompletedNCT04498182Phase 2Results posted
- Comparison Between iLux and LipiFlow in the Treatment of Meibomian Gland Dysfunction (MGD): A 12-month, Multicenter StudyCompletedNCT03956225Not applicableResults posted
- Clinical Outcomes Following Treatment With SYSTANE® BALANCECompletedNCT02776670Not applicableResults posted
- Clinical Evaluation of Systane® Balance in Dry Eye SubjectsTerminatedNCT02511379Not 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
- Clinical Evaluation of Systane® Gel Drops in Dry Eye SubjectsCompletedNCT02380248Not applicableResults posted
- Clinical Outcomes Following Treatment With Systane® Balance in Dry Eye SubjectsCompletedNCT01967147Not applicableResults posted
- Clinical Evaluation of Systane® ULTRA Compared to OPTIVE® in Ocular Surface StainingCompletedNCT01863368Not applicableResults posted
- Efficacy and Safety Study of FID 119515ACompletedNCT01833117Not applicableResults posted
- SYSTANE® Family - Meibomian DeficiencyCompletedNCT01733745Not applicableResults posted
- SYSTANE® BALANCE Symptoms (OSDI) & Inflammatory BiomarkersCompletedNCT01733732Not applicableResults posted
- The Effect of SYSTANE® BALANCE on Tear Film Break Up Time in Dry Eye SubjectsCompletedNCT01718028Not applicableResults posted
- Evaluation of SYSTANE® BALANCE in Dry Eye Subjects With Lipid DeficiencyCompletedNCT01688726Not applicableResults posted
- Clinical Evaluation of a Daily Disposable Contact Lens in Symptomatic Weekly/Monthly Lens WearersCompletedNCT01614600Not applicableResults posted
- Effect of Contact Lenses on Tear Osmolarity in a Controlled Low Humidity ChamberCompletedNCT01482312Not applicableResults posted
- Sodium Hyaluronate Ophthalmic Solution, 0.18% for Treatment of Dry Eye SyndromeCompletedNCT01382225Phase 3Results posted
- ESBA105 in Patients With Severe Dry EyeCompletedNCT01338610Phase 2Results posted
- Evaluation of Anti-Inflammatory Treatment in Dry Eye PatientsCompletedNCT01276223Phase 2Results posted
- Acute Comfort and Blurring Profile Evaluation of Marketed Lubricant Eye DropsCompletedNCT00756093Not applicableResults posted
- Acute Comfort and Blur of Systane Ultra and SystaneCompletedNCT00748865Not applicableResults posted
- Punctal Plug Study to Determine the Safety and Retention Times of Various Lengths of Canalicular Stents in VolunteersCompletedNCT00743249Not applicableResults posted
- Evaluation of SYSTANE Ultra Lubricant Eye DropsCompletedNCT00702377Not applicableResults posted
- Tobramycin Tear ConcentrationsCompletedNCT00695435Phase 1Results 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
- Acute Comfort and Blur of Systane and OptiveCompletedNCT00568386Not applicableResults posted
- Evaluation of Tears Naturale® Free and Tears Naturale® II Lubricant Eye DropsCompletedNCT07540884Not applicable
- An Evaluation of the Safety and Tolerability of Ocular LubricantsCompletedNCT07238699Not applicable
- Evaluation of the Safety and Tolerability of Ocular LubricantsTerminatedNCT06571656Not applicable
- Evaluation of Reflex Tear ProductionTerminatedNCT06565624Not applicable
- Systane® Hydration PF and Systane® Hydration PreservedCompletedNCT05932238Not applicable
- Evaluation of Safety and Tolerability of Investigational Ocular LubricantsCompletedNCT05888519Not applicable
- 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
- Systane Hydration in Subjects Undergoing Cataract SurgeryCompletedNCT05056233Not applicable
- Systane Complete Multi-symptom ReliefCompletedNCT05056155Not applicable
- Evaluation of Comfort in Subjects With Moderate Dry Eye DiseaseCompletedNCT04830956Not applicable
- Study of Efficacy and Tolerability of SYSTANE Complete in Patients With Dry Eye DiseaseCompletedNCT03492541Not applicable
- Optimization of Assessment and Grading for Lid Wiper EpitheliopathyCompletedNCT01611922
- In Vivo Measurement of Corneal Epithelial Changes in Dry Eye PatientsCompletedNCT01483989Not applicable
- Comparative Efficacy of SYSTANE® ULTRA vs Optive™ in Improving Tear Film Break-up TimeWithdrawnNCT01417013Not applicable
- Evaluation of Extended Tear Film Break Up Time (TFBUT) With an Ocular EmulsionCompletedNCT01368198Not applicable
- A Multi-Site Post Marketing Surveillance Study for Systane in Indian PatientsCompletedNCT01311609Phase 4
- A Clinical Evaluation of an Investigational Lubricant Eye Gel (FID 115958D)CompletedNCT01294956Not applicable
- Residence Time Evaluation of Systane Ultra Lubricant Eye Drops vs. Hialid and SalineCompletedNCT01252121Not applicable
- An Open-Label, Single-Center Study Evaluating the Effect of Systane Balance on Video Ocular Protection Index (OPI) and Blink Patterns in Patients Diagnosed With Dry EyeCompletedNCT01223040Not applicable
- Evaluating Safety and Efficacy of FID 112903 Post Discontinuation of Long-term Use of RESTASIS® (Cyclosporine Ophthalmic Emulsion) 0.05%CompletedNCT01198782Phase 4
- An Evaluation of the Nighttime Retention of Effect of an Investigational Lubricant Eye Drop (FID 115958D)CompletedNCT01165164Not applicable
- To Evaluate the Physical Effects of Systane(R) Lubricant Eye Drops Compared to Refresh Tears(R) Lubricant Eye DropsCompletedNCT01160133Not applicable
- An Evaluation of the Daytime Use of an Investigational Lubricant Eye DropCompletedNCT01139372Not applicable
- Efficacy of Systane Ultra in Post Menopausal Women With Dry EyeCompletedNCT01105910Phase 4
- Efficacy of Systane Balance to Stabilize the Tear Film in Dry Eye SubjectsCompletedNCT01086774Phase 4
- Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Lubricant Eye GelCompletedNCT01077011Not applicable
- Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Eye OintmentCompletedNCT01076998Not applicable
- Evaluation of an Investigational Lubricant Eye Drop on Lipid Layer ThicknessCompletedNCT01066988Not applicable
- Evaluation of the Repeated Usage of Systane Ultra EyedropCompletedNCT01051804Phase 4
- An Evaluation of the Safety and Efficacy of FID 114657CompletedNCT01030237Not applicable
- Tear Film Break-Up Time Evaluation of FID 114657CompletedNCT01023464Not applicable
- Clinical Evaluation of the Causes of Contact Lens Related Dry EyeCompletedNCT00995189Not applicable
- Acute Comfort and Haze Profile of FID 114657CompletedNCT00983203Not applicable
- Barrier Function Measurement in Dry Eye Patients After Using Systane Ultra for 30 DaysCompletedNCT00946777Not applicable
- Evaluate the Ability of Systane Ultra to Improve Subjective Symptoms of Ocular Irritation Post 60 Min. Athletic Performance.CompletedNCT00938951Not applicable
- A Study of AL-38583 Ophthalmic Solution 0.05%, 0.010% Versus AL-38583 Vehicle for Dry EyeCompletedNCT00893139Phase 2
- Evaluation of FID 114657 on Tear Film Lipid Layer ThicknessCompletedNCT00848068Not applicable
- A Study of Hydroxypropyl Guar Galactomannan 0.25% (HPGG) Versus Vehicle in Dry Eye PatientsCompletedNCT00840268Phase 2
- Systane Clinical Experience StudyCompletedNCT00818909Phase 4
- Kynex Versus Refresh Plus Study in Subject With Dry EyeCompletedNCT00809198Phase 4
- Residence Time Evaluation of Marketed OTC Ophthalmic ProductsCompletedNCT00804791Not applicable
- A 2-week Clinical Comparison of SYSTANE® Ultra to Sensitive Eyes Rewetting Drops in Contact Lens Wearing Patients.CompletedNCT00769665
- Clinical Pharmacological Study of AL-43546 Ophthalmic Product in Subjects With Shortened Tear Film Break Up TimeCompletedNCT00760045Phase 2
- Evaluate Artificial Tear Efficacy in Moderate to Severe Dry EyeCompletedNCT00724412Phase 4
- Phase II Study of AL-2178 (FID 109980) in the Treatment of Dry EyeCompletedNCT00471419Phase 3
- Safety/Efficacy of Systane Free vs Refresh LiquigelCompletedNCT00348517Not applicable
- Safety/Efficacy of Systane Free vs Refresh TearsCompletedNCT00348322Not applicable
- Product Preference With Systane Compared to Artificial Tears on Frequency of Drop UseCompletedNCT00347984Not applicable