Effectiveness Study of Zymar Versus Vigamox for Preoperative Sterilization of the Ocular Surface After Loading Dose
NCT00347828 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2006-07-04
Summary
The purpose of this study is to analyze the effect of Zymar and Vigamox on ocular surface bacteria. We believe that Zymar will eradicate more ocular surface bacteria than Vigamox.
Conditions
- Eye Infection
- Infection
Interventions
- DRUG
-
Moxifloxacin ophthalmic solution 0.5%
- DRUG
-
Gatifloxacin ophthalmic solution 0.3%
Sponsors & Collaborators
-
Allergan
collaborator INDUSTRY -
Ophthalmic Consultants of Boston
lead OTHER
Principal Investigators
-
Michael B Raizman, B.A./M.D. · Ophthalmic Consultants of Boston
-
Sandra Y Cho, B.A./M.D. · New England Eye Center/Tufts-New England Medical Center
-
Rahul Mandiga, B.S. · New England Eye Center/Tufts-New England Medical Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- DOUBLE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 25 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2006-06-30
- Completion
- 2006-06-30
Countries
- United States
Study Locations
More Related Trials
-
A Phase 3 Study to Evaluate the Efficacy and Safety of Pimecrolimus 0.3% Ophthalmic Ointment
NCT06400511 ·Status: TERMINATED ·Phase: PHASE3
-
Study to Evaluate the Safety and Tolerability of PRO-231 Versus VIGAMOXI® on the Ocular Surface of Healthy Subjects
NCT06363292 ·Status: COMPLETED ·Phase: PHASE1
-
The Efficacy of Permethrin 5%, Fusidic Acid 1% and Synthomycine 5% for Demodex - Blepharitis
NCT03105505 ·Status: UNKNOWN ·Phase: PHASE4
-
Combination Treatment of 5% Natamycin and 1% Voriconazole in Fungal Keratitis
NCT03230058 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
A Placebo Controlled Comparison of Topical Zirgan Versus Genteal Gel for the Treatment of Adenovirus Conjunctivitis
NCT01533480 ·Status: COMPLETED ·Phase: PHASE4
-
Moxifloxacin AF Ophthalmic Solution for Treatment of Bacterial Conjunctivitis
NCT00759148 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of Auriclosene (NVC-422) in the Treatment of Bacterial Conjunctivitis
NCT01877694 ·Status: COMPLETED ·Phase: PHASE2
-
Study of the Progression of Bacterial Conjunctivitis Symptoms Upon Antibiotic Treatment
NCT00798577 ·Status: COMPLETED ·Phase: PHASE4
-
A Safety Study of of AG-920 Sterile Topical Ophthalmic Solution
NCT05501860 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety Assessment of Azyter® Eye Drops (T1225) in Patients With Blepharitis
NCT01089608 ·Status: COMPLETED ·Phase: PHASE2
-
Safety, Efficacy, Tolerability and Pharmacokinetics of AGN-223575 Ophthalmic Suspension in Patients With Dry Eye Disease
NCT02435914 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Efficacy of AL-15469A 0.5% / AL-6515 0.3% Ophthalmic Suspension for Treatment of Bacterial Conjunctivitis
NCT01238783 ·Status: WITHDRAWN ·Phase: PHASE2
-
Therapeutic Exploratory Study of Comparing Natamycin and Voriconazole to Treat Fungal Corneal Ulcer
NCT00557362 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Study of the Safety and Efficacy of Gatifloxacin in Patients With Bacterial Conjunctivitis
NCT00518089 ·Status: COMPLETED ·Phase: PHASE3
-
A Phase 2b Study Evaluating the Safety and Efficacy of AR-15512 Ophthalmic Solution for the Treatment of Dry Eye Disease
NCT04498182 ·Status: COMPLETED ·Phase: PHASE2
-
Impact of XDEMVY® on Demodex Blepharitis in Soft Contact Lens Wearers
NCT06182358 ·Status: COMPLETED ·Phase: PHASE4
-
Effect of an Exploratory Vehicle on Meibomian Gland Dysfunction in Patients With Demodex
NCT06054217 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Four Week, Open-Label Study of Azithromycin Ophthalmic Solution, 1% (P08641)
NCT01220258 ·Status: TERMINATED ·Phase: PHASE2
-
A Study of the Safety and Anesthetic Effect of AG-920 Topical Ophthalmic Solution
NCT04829344 ·Status: COMPLETED ·Phase: PHASE3
-
A Four Week Study of Azithromycin Ophthalmic Solution, 1% Versus Vehicle in Subjects With Blepharitis (P08636)
NCT01269658 ·Status: TERMINATED ·Phase: PHASE2
-
EffiCacy, Safety and ToLErability of a Novel Ocular ANtiseptic for Ocular Use (CLEAN)
NCT05127525 ·Status: TERMINATED ·Phase: PHASE3
-
Study of Two Marketed Ocular Anti-Allergy Medications in Subjects With Allergic Conjunctivitis
NCT00534794 ·Status: COMPLETED ·Phase: PHASE4
-
Comparative Study in the Efficacy of Topical Besifloxocin With Erythromycin for the Management of Acute Blepharitis
NCT01478256 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy of Zylet vs. Lotemax for the Treatment of Ocular Surface Inflammation/MGD/Blepharitis
NCT01456780 ·Status: COMPLETED ·Phase: PHASE4
-
Concentration of Besifloxacin, Gatifloxacin, and Moxifloxacin in Human Conjunctiva After Topical Instillation
NCT00905762 ·Status: COMPLETED ·Phase: PHASE1