Comprehensive Eye Care, Ltd.

Washington, Missouri 63090-3010

1 studies enrolling now · 29 studies all time

What they study most

Anterior Uveitis, Blepharitis, Cataract, Cataract Extraction, Corneal Edema After Cataract Surgery, Dry Eye, Dry Eye Disease, Dry Eye Disease (DED), Dry Eye Syndromes, Fuchs Endothelial Corneal Dystrophy, Glaucoma, Glaucoma and Ocular Hypertension

Studies at this site

• An Exploratory Efficacy and Safety Study of DFL24498 Topical Ophthalmic Solution Compared With Vehicle in Participants With Dry Eye Disease — Recruiting now
• A Multicenter Study Assessing the Efficacy and Safety of STN1010904 Ophthalmic Suspension 0.03% and 0.1% Compared With Vehicle in Subjects With Fuchs Endothelial Corneal Dystrophy (FECD) — Completed
• A Study to Investigate the Safety and Efficacy of Ripasudil (K-321) Eye Drops After Cataract Surgery — Completed
• A Study Evaluating the Safety and Efficacy of a Fixed-Dose Combination for Dry Eye Disease — Completed
• Phase 2: VVN461 Ophthalmic Solution for Post -Operative Ocular Inflammation After Cataract Surgery — Completed
• A Study to Confirm the Efficacy and Safety of K-161 Ophthalmic Solution for Treatment of Moderate to Severe Dry Eye Disease — Completed
• Efficacy and Safety Assessment of T4032 (Unpreserved Bimatoprost 0.01%) Versus Lumigan® 0.01% in Ocular Hypertensive or Glaucomatous Patients — Completed
• Study Assessing the Efficacy and Safety of STN1013600 Ophthalmic Solution 0.1% and 0.3% Compared With Placebo in Subjects With Presbyopia — Completed
• DE-117 Spectrum 5 Study — Completed
• A Phase III Study Assessing the Efficacy and Safety of DE-117 Ophthalmic Solution Compared With Timolol Maleate Ophthalmic Solution 0.5% in Subjects With Glaucoma or Ocular Hypertension - Spectrum 4 Study — Completed
• Study of OT-101 in Treating Myopia — Running, not enrolling
• Efficacy and Safety of APP13007 for Treatment of Inflammation and Pain After Cataract Surgery — Completed
• EyeKon Medical Inc. Capsular Tension Ring Study — Status unconfirmed
• Clobetasol Propionate Ophthalmic Nanoemulsion 0.05% for the Treatment of Inflammation and Pain Associated With Cataract Surgery (CLOSE-2) — Completed
• Study to Evaluate the Safety and Efficacy of SDP-4 in Subjects With Dry Eye Disease (DED) — Completed
• Efficacy and Safety Study of a Steroid/Antibiotic Combination Eyedrop to Treat Non-Bacterial Blepharitis — Completed
• A Study to Evaluate Efficacy and Safety of Lifitegrast in Subjects With Dry Eye (OPUS-3) — Completed
• Hydrophilic Acrylic Intraocular Lens — Withdrawn before enrolling
• A Study of the Concurrent Use of AGN-190584 and AGN-199201 in Participants With Presbyopia — Completed
• A Safety and Efficacy Study of Refresh Optive® Gel Drops in Patients With Dry Eye Disease — Completed
• Safety, Efficacy, Tolerability and Pharmacokinetics of AGN-223575 Ophthalmic Suspension in Patients With Dry Eye Disease — Completed
• Evaluation of P-321 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye Disease — Stopped early
• A Study to Evaluate the Safety and Efficacy of EV06 Ophthalmic Solution in Improving Vision in Subjects With Presbyopia — Completed
• A Study of AGN-195263 for the Treatment of Meibomian Gland Dysfunction — Completed
• A Phase 2 Single-Masked, Randomized Study of Latanoprost PPDS in Ocular Hypertension or Open-Angle Glaucoma — Completed
• The Effects of Azithromycin Ophthalmic Solution, 1% Versus Placebo in Subjects With Blepharitis During a Four-Week Treatment Period (P08638) — Completed
• A Dose Evaluation Study of the Effect of Plug Placement on the Efficacy and Safety of the Latanoprost Punctal Plug Delivery System (L-PPDS) in Subjects With Ocular Hypertension or Open-Angle Glaucoma — Completed
• Safety and Efficacy Study of Iontophoretic Dexamethasone Phosphate Ophthalmic Solution to Treat Non-Infectious Anterior Segment Uveitis — Completed
• Safety and Efficacy Study of Iontophoresis and Dexamethasone Phosphate to Treat Anterior Uveitis — Completed