Bausch & Lomb Incorporated
Bausch & Lomb Incorporated
Explore linked clinical trials.17 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| BL-RX01-TFSTAB-1402 | dry eye syndrome, eye disorder, lacrimal apparatus disorder | Recruiting | Phase 4 | 2026-08-27 | NCT07790211 | |
| BL1107 Response and Intensity Guided Dosing for Hyperemia Resolution Trial | dry eye syndrome, eye disorder, lacrimal apparatus disorder | Not yet recruiting | Phase 2 | 2026-08-21 | NCT07778888 | |
| A Single Center, Open-Label Study to Evaluate the Ability of the TearScience™ LipiView™ II Ocular Surface Interferometer and the Keratograph® 5M to Detect Tear Film Stability Utilizing Miebo® | dry eye syndrome, eye disorder, lacrimal apparatus disorder | Active, not recruiting | Phase 4 | 2026-07-29 | NCT07722624 | |
| A Multicenter, Open-Label Study to Evaluate Perioperative Treatment of Dry Eye With Miebo® in Subjects Undergoing LASIK | dry eye syndrome, eye disorder, lacrimal apparatus disorder | Recruiting | Phase 4 | 2026-06-24 | NCT07650708 | |
| Efficacy of a Novel Myopia Defocus Spectacle Lens in School-Aged Children | eye disorder, myopia, refractive error | Active, not recruiting | Not applicable | 2026-06-03 | NCT07511387 | |
| Oral Health In Cirrhosis of the Liver (ORACLE) | Fibrosis, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Stomatognathic Diseases, cirrhosis of liver, mouth disorder, periodontal disorder | Active, not recruiting | Not stated | 2026-04-03 | NCT06052150 | |
| This is a Single Center, Open-label Prospective Study to Evaluate the Effect of Xiidra® (Lifitegrast Ophthalmic Solution 5.0%) on Tear Film Biomarkers in Dry Eye | dry eye syndrome, eye disorder, lacrimal apparatus disorder | Not yet recruiting | Phase 4 | 2026-03-24 | NCT07490535 | |
| Treatment of Ocular Discomfort in Glaucoma Patients Using Multiple Topical Medications | eye disorder, glaucoma, ocular hypertension | Recruiting | Not stated | 2026-03-13 | NCT04354545 | |
| A Study to Evaluate the Use of Topical Ocular BL1332 for the Management of Postoperative Ocular Pain Following Photorefractive Keratectomy | Neurologic Manifestations, Pain, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Postoperative Complications, Postoperative Pain, Signs and Symptoms | Not yet recruiting | Phase 2 | 2026-02-17 | NCT07412496 | |
| A Study to Investigate the Safety and Effectiveness of the Technolas® TENEO 317 Model 2 Excimer Laser for Laser In Situ Keratomileusis (LASIK) Surgery to Treat Myopia or Myopic Astigmatism | Myopic Astigmatism, astigmatism, eye disorder, refractive error | Not yet recruiting | Not applicable | 2026-01-30 | NCT07377474 | |
| A Study to Assess Safety, Tolerability, and Pharmacokinetics of Ascending Concentrations of Topical Ocular BL1332 in Healthy Volunteers | Eye Manifestations, Eye Pain, Neurologic Manifestations, Pain, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, eye disorder | Active, not recruiting | Phase 1 | 2026-01-27 | NCT06978244 | |
| IC-8 Apthera IOL New Enrollment Post Approval Study | cataract, eye disorder, lens disorder, presbyopia, refractive error | Recruiting | Not stated | 2026-01-12 | NCT06060041 | |
| Revive Toric RWE Study | astigmatism, eye disorder, refractive error | Not yet recruiting | Not stated | 2025-11-28 | NCT06785194 | |
| Effectiveness and Safety of the TENEO 317 Model 2 Excimer Laser to Treat Myopia With or Without Astigmatism by Transepithelial Photorefractive Keratectomy | eye disorder, myopia, refractive error | Not yet recruiting | Not applicable | 2025-06-15 | NCT06618547 | |
| A Study to Evaluate the Safety and Efficacy of the Bausch + Lomb Myopia Control Lens for the Correction of Myopic Ametropia and Slowing the Progression of Myopia in Children | eye disorder, myopia, refractive error | Recruiting | Not applicable | 2025-06-15 | NCT06305663 | |
| Effect of Defocus in Soft Contact Lenses on Internal Retinal Vascularization | eye disorder, myopia, refractive error | Active, not recruiting | Not applicable | 2025-03-27 | NCT06527274 | |
| A Study to Evaluate Corneal Endothelial Cell Density (ECD) in Subjects With Dry Eye Disease (DED) Administering Miebo® (Perfluorohexyloctane Ophthalmic Solution) for 12 Months. | dry eye syndrome, eye disorder, lacrimal apparatus disorder | Active, not recruiting | Phase 4 | 2024-12-17 | NCT06565650 |