Systane Ultra Versus Maxidex Versus Saline
NCT01775540 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36
Last updated 2013-01-25
Summary
This study was to evaluate the healing action on the eye surface of the artificial tear Systane® ULTRA as compared to two other eyedrops: Maxidex and Saline solution. Dry eye disease leads to inflammation of the eye surface and treating dry eyes with artificial tears may lead to reduction in this inflammation and improvement of symptoms and signs.
Conditions
Interventions
- DRUG
-
Systane Ultra
Artificial tear Eyedrop, 1 drop used QID for 4 weeks
- DRUG
-
Saline solution
Saline solution,1 drop used QID for 4 weeks
- DRUG
-
Maxidex
Eyedrop-1 drop QID for 4 weeks
Sponsors & Collaborators
-
Alcon Research
collaborator INDUSTRY -
Icahn School of Medicine at Mount Sinai
lead OTHER
Principal Investigators
-
Penny Asbell, MD, MBA, FACS · Icahn School of Medicine at Mount Sinai
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-05-31
- Primary Completion
- 2012-10-31
- Completion
- 2012-10-31
Countries
- United States
Study Locations
More Related Trials
-
SYSTANE® Family - Meibomian Deficiency
NCT01733745 ·Status: COMPLETED ·Phase: NA
-
Clinical Study Aimed At Evaluating the Safety and Efficacy of Tear Substitute Formulations in the Treatment of Dry Eye Disease.
NCT06633471 ·Status: NOT_YET_RECRUITING ·Phase: EARLY_PHASE1
-
Efficacy of a New Nanoemulsion Artificial Tear Targeting Dry Eye Disease
NCT06188260 ·Status: COMPLETED ·Phase: PHASE2
-
To Evaluate the Physical Effects of Systane(R) Lubricant Eye Drops Compared to Refresh Tears(R) Lubricant Eye Drops
NCT01160133 ·Status: COMPLETED ·Phase: NA
-
Evaluation of SYSTANE® BALANCE in Dry Eye Subjects With Lipid Deficiency
NCT01688726 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Clinical Outcomes After the Use of SYSTANE® HYDRATION
NCT02470429 ·Status: COMPLETED ·Phase: NA
-
Comparison of Systane Free vs. Saline in the Treatment of Dry Eye
NCT00388791 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of the Ophthalmic Solution PRO-087 Versus Systane ® Ultra and Ultra Preservative Free (087LATAMFIV)
NCT03223909 ·Status: COMPLETED ·Phase: PHASE4
-
Clinical Outcomes Following Treatment With Systane® Balance in Dry Eye Subjects
NCT01967147 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of Systane® Gel Drops in Dry Eye Subjects
NCT02380248 ·Status: COMPLETED ·Phase: NA
-
Study of Efficacy and Tolerability of SYSTANE Complete in Patients With Dry Eye Disease
NCT03492541 ·Status: COMPLETED ·Phase: NA
-
Effects of Dry Eye Treatments on the Ocular Surface
NCT01797822 ·Status: COMPLETED ·Phase: PHASE4
-
SYSTANE® PRO vs. MIEBO™ in Dry Eye Disease
NCT07243275 ·Status: RECRUITING ·Phase: PHASE4
-
Artificial Tears Study in Mild to Moderate Dry Eye Patients
NCT00607776 ·Status: COMPLETED ·Phase: PHASE2
-
A Dose-Ranging Clinical Study to Assess the Safety and Efficacy of Subconjunctival Injection of Sirolimus in Patients With Dry Eye in the Controlled Adverse Environmental (CAE) Model
NCT00814944 ·Status: COMPLETED ·Phase: PHASE2
-
Comprehensive Study on Dry Eye and Ocular Surface Disease Prior and After Cataract Surgery
NCT04711642 ·Status: UNKNOWN ·Phase: PHASE3
-
Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects
NCT01010282 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Blink Tears and Systane Concomitant With Restasis for the Treatment of Dry Eye Symptoms
NCT00565669 ·Status: COMPLETED ·Phase: NA
-
A Safety, Tolerability and Pharmacokinetics Study of R932348 Eye Drops in Patients With Dry Eye Disease
NCT01733992 ·Status: COMPLETED ·Phase: PHASE1
-
Tear Film Break-up Time After Instillation of Artificial Tears
NCT00681265 ·Status: COMPLETED ·Phase: NA
-
Non-invasive Tear Film Dynamic Measurements in Normal, MGD and ADDE Subjects After Saline Instillation
NCT01128049 ·Status: COMPLETED ·Phase: NA
-
The Efficacy of an Ocular Emulsion in Meibomian Gland Dysfunction
NCT01207752 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Anti-Inflammatory Treatment in Dry Eye Patients
NCT01276223 ·Status: COMPLETED ·Phase: PHASE2
-
Dextenza With ILUX for Treatment of MGD
NCT04658927 ·Status: COMPLETED ·Phase: PHASE4
-
Study to Evaluate the Safety and Tolerability of PRO-190 Ophthalmic Solution Compared to Systane Ultra® on the Ocular Surface.
NCT06379685 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1