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Active clinical trials for "Ocular Hypertension"

Results 291-300 of 587

A Safety and Efficacy Study of Bimatoprost 0.01% in Primary Open-Angle Glaucoma (POAG) or Ocular...

GlaucomaOpen-Angle1 more

This study will evaluate the safety and efficacy of bimatoprost 0.01% in subjects with elevated intraocular pressure (IOP) due to primary open-angle glaucoma (POAG) or ocular hypertension (OH).

Completed2 enrollment criteria

SYL040012. Tolerance and Effect on Intraocular Pressure in Subjects With Intraocular Pressure (IOP)...

GlaucomaOcular Hypertension

The aim of this study is to evaluate the tolerance and effect on unmedicated subjects with elevated IOP.

Completed29 enrollment criteria

Safety and Efficacy of Triple Combination Therapy in Patients With Glaucoma or Ocular Hypertension...

GlaucomaOcular Hypertension

This study will investigate the safety and efficacy of Triple Combination Therapy (bimatoprost/brimonidine tartrate/timolol fixed combination ophthalmic solution) in patients with glaucoma or ocular hypertension who have elevated intraocular pressure (IOP) on brimonidine/timolol ophthalmic solution.

Completed8 enrollment criteria

Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open-Angle Glaucoma or...

GlaucomaOpen-Angle1 more

This study will evaluate the safety and efficacy of Triple Combination Therapy compared with Fixed Combination brimonidine tartrate/timolol ophthalmic solution in patients with primary open-angle glaucoma or ocular hypertension.

Completed7 enrollment criteria

A Safety Study of Bimatoprost in Patients With Glaucoma or Ocular Hypertension

GlaucomaOcular Hypertension

This safety study will evaluate bimatoprost 0.01% and 0.03% in patients with glaucoma or ocular hypertension (OHT).

Completed3 enrollment criteria

A Phase 2 Single-Masked, Randomized Study of Latanoprost PPDS in Ocular Hypertension or Open-Angle...

Ocular HypertensionOpen-Angle Glaucoma

Determine efficacy of the latanoprost punctal plug. Effect of configuration of L-PPDS placement on efficacy will also be examined.

Completed30 enrollment criteria

AR-12286 Fixed Dose Combination to Lower Elevated Intraocular Pressure

GlaucomaOcular Hypertension

This is a double-masked, randomized, controlled study assessing the safety and ocular hypotensive efficacy of two AR 12286/travoprost fixed-dose combination products compared to Travatan® Z in patients with elevated intraocular pressure

Completed25 enrollment criteria

Efficacy and Tolerability of AZARGA® as Replacement Therapy in Patients on COMBIGAN® Therapy in...

GlaucomaOcular Hypertension1 more

The purpose of this study was to assess the efficacy and tolerability of changing to AZARGA® from prior brimonidine 0.2%/timolol 0.5% fixed combination (COMBIGAN®) therapy in patients with open-angle glaucoma or ocular hypertension and uncontrolled intraocular pressure (IOP).

Completed21 enrollment criteria

Subjects With Open-angle Glaucoma, Pseudoexfoliative Glaucoma, or Ocular Hypertension Naïve to Medical...

Open-angle Glaucoma

Evaluation of the intraocular pressure (IOP) lowering effect of two iStent devices versus medical therapy in eyes of subjects with primary open-angle glaucoma, pseudoexfoliative glaucoma, or ocular hypertension naïve to medical and surgical therapy.

Completed4 enrollment criteria

A Dose Evaluation Study of the Effect of Plug Placement on the Efficacy and Safety of the Latanoprost...

GlaucomaOcular Hypertension (OH)

The purpose of this study is to determine the effect of plug placement on the efficacy, safety and duration of effect of the L-PPDS (latanoprost punctal plug delivery system).

Completed8 enrollment criteria
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