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Active clinical trials for "Ocular Hypertension"

Results 261-270 of 587

Study of Brinzolamide and Timolol When Added to Travoprost in Primary Open-angle Glaucoma or Ocular...

Primary Open-angle GlaucomaOcular Hypertension1 more

The purpose of the study is to compare the efficacy and safety of Timolol 0.5% solution to Brinzolamide 1% each given twice daily when added to Travoprost 0.004% given each evening.

Completed2 enrollment criteria

Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients With Glaucoma or...

Ocular Hypertension

The purpose of this study is to assess the safety and efficacy of Bimatoprost/Timolol Fixed Combination in patients with glaucoma or ocular hypertension

Completed4 enrollment criteria

Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients Wtih Glaucoma or...

Ocular Hypertension

The purpose of this study is to assess the safety and efficacy of Bimatoprost/Timolol Fixed Combination in the treatment of glaucoma or ocular hypertension

Completed4 enrollment criteria

Phase 3 Study to Evaluate IOP Lowering Therapy in Open Angle Glaucoma and Ocular Hypertension C-01-69...

Open-Angle GlaucomaOcular Hypertension

To compare intraocular pressure lowering effectiveness of a combination drug vs. two individual drugs dosed alone.

Completed1 enrollment criteria

A 6-week Safety & Efficacy Study of Combination Intraocular Pressure-lowering Therapy in Patients...

GlaucomaOpen-angle1 more

To compare the intraocular pressure(IOP)-lowering efficacy of morning or evening instillations of a combination IOP-lowering therapy in patients with open-angle glaucoma or ocular hypertension.

Completed1 enrollment criteria

Efficacy And Safety Of Xalatan Compared To Usual Care In Patients With Open Angle Glaucoma Or Ocular...

Ocular HypertensionGlaucoma1 more

The primary purpose is to compare the intraocular pressure reducing effect of Xalatan with that of usual care over 36 months. Safety and health care utilization will be evaluated.

Completed3 enrollment criteria

Safety and Efficacy Study of BETOPTIC S 0.25% and Timolol Gel-forming Solution 0.25% and 0.5% in...

GlaucomaOcular Hypertension

The purpose of this study is to evaluate the safety and efficacy of BETOPTIC S and Timolol Gel-forming solution in pediatric patients. Patients will dose with study drug at 8 am and 8 pm daily for twelve weeks. Patients will have vision tested, slit lamp exam, blood pressure and pulse checks at each visit. Patients will have a dilated fundus exam and corneal measurements taken at first and last visit.

Completed15 enrollment criteria

Cosopt Versus Xalatan

Open-Angle GlaucomaOcular Hypertension

To compare the 24-hour efficacy and safety, measured every three hours, of the dorzolamide/timolol fixed combination given twice daily versus latanoprost and placebo each given once daily.

Completed5 enrollment criteria

A Study to Evaluate the Long Term Safety of OTX-TP (Sustained Release Travoprost) Intracanalicular...

Open Angle Glaucoma and Ocular Hypertension

To evaluate the long term safety of repeat dose OTX-TP, a sustained release travoprost drug product, placed in the canaliculus of the eyelid in the treatment of subjects with open-angle glaucoma or ocular hypertension.

Completed7 enrollment criteria

Study of ST266 Given by Intranasal Delivery in Glaucoma Suspect Subjects

Ocular Hypertension

The primary objective of this trial is to assess the safety of ST266 given by non-invasive intranasal trans-cribriform delivery to glaucoma suspect subjects with ocular hypertension, optic nerve cupping, or family history of glaucoma.

Completed34 enrollment criteria
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