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Ocular Hypertension clinical trials

View clinical trials related to Ocular Hypertension.

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NCT ID: NCT00864838 Completed - Clinical trials for Diabetic Retinopathy

Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis for Ocular Hypertension Control After Intravitreal Bevacizumab

Start date: June 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effects of anterior chamber paracentesis, brimonidine and oral acetazolamide to reduce intra-ocular pressure variations after intravitreal bevacizumab injection.

NCT ID: NCT00856622 Completed - Glaucoma Clinical Trials

A Study Demonstrating The Effect Of Latanoprost In Combination With Timolol, Latanoprost Alone And Timolol Alone On Eye Pressure In Open Angle Glaucoma Or Ocular Hypertension In Patients

Start date: August 1997
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate that fixed combination of latanoprost and timolol (PhXA41) has better IOP lowering effect than the individual monotherapies.

NCT ID: NCT00848536 Completed - Ocular Hypertension Clinical Trials

Efficacy Study of Travoprost APS Versus TRAVATAN

Start date: March 2009
Phase: Phase 3
Study type: Interventional

A Multi-Center Double-masked Study of the Safety and Efficacy of Travoprost APS Compared to TRAVATAN in Patients with Open-angle Glaucoma or Ocular Hypertension

NCT ID: NCT00847483 Completed - Glaucoma Clinical Trials

Comparison of Latanoprost With Travoprost and Bimatoprost in Patients With Elevated IOP. A 12-weeks, Masked Evaluator, Phase IV Multi-center Study in the US

XLT
Start date: January 2002
Phase: Phase 4
Study type: Interventional

Compare the IOP lowering properties of latanoprost, travoprost and bimatoprost

NCT ID: NCT00846989 Completed - Glaucoma Clinical Trials

Efficacy, Tolerability and Safety of RKI983 (0.05% & 0.10%) vs Xalatan in Patients With POAG or Ocular Hypertension

Start date: January 2009
Phase: Phase 1/Phase 2
Study type: Interventional

This purpose of this study is to access the efficacy, tolerability and safety of RKI983 (0.05% and 0.10%) ophthalmic solution bid versus once daily latanoprost 0.005%, in patients with POAG or ocular hypertension.

NCT ID: NCT00845299 Completed - Glaucoma Clinical Trials

Study of the Effects of Artificial Tears on the Response to the Latanoprost Punctal Plug Delivery System in Subjects With Ocular Hypertension or Open-Angle Glaucoma

Start date: January 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effect of artificial tears preserved with Benzalkonium Chloride (AT-BAK) on the IOP response to the L-PPDS and to evaluate the safety of the L-PPDS in subjects with OH or OAG following treatment.

NCT ID: NCT00838721 Completed - Ocular Hypertension Clinical Trials

Evaluation of Pascal Laser Trabeculoplaty

PLT
Start date: March 2008
Phase: N/A
Study type: Interventional

Laser Trabeculoplasty has been shown to be effective in lowering intraocular pressure (IOP) in patients with primary open-angle glaucoma (POAG). Although initially demonstrated with the Argon laser (ALT), several other laser systems have also been employed with comparable efficacy. Recently, Selective Laser Trabeculoplasty (SLT) has been shown to lower intraocular pressure comparable to ALT. The advantage of SLT is that the target eye structure, the trabecular meshwork, remains intact with minimal damage at the cellular level. In contrast, ALT lowers IOP at the expense of scarring of the trabecular meshwork. The purpose of this study is to evaluate the efficacy of lowering IOP with Pascal Laser Trabeculoplasty (PLT) employing reduced energy levels compared to ALT and a computer guided pattern of laser treatment applications.

NCT ID: NCT00834171 Completed - Ocular Hypertension Clinical Trials

A Retrospective Evaluation of the Intraocular Pressure Spikes With Loteprednol and Loteprednol/Tobramycin

Start date: January 2009
Phase: N/A
Study type: Observational

Patient charts will be reviewed to evaluate the incidence of intraocular pressure spikes while on Loteprednol etabonate ophthalmic suspension 0.5%, Loteprednol etabonate (0.5%) and tobramycin (0.3%)

NCT ID: NCT00828906 Completed - Ocular Hypertension Clinical Trials

DuoTrav® Eye Drops As Replacement Therapy Program

Start date: February 2009
Phase: Phase 4
Study type: Interventional

To evaluate the effectiveness of DuoTrav Eye Drops in gaining or maintaining control of target Intraocular Pressures (tIOP) in patients diagnosed with, and being treated for, open-angle glaucoma (OAG) or ocular hypertension (OH).

NCT ID: NCT00825396 Completed - Ocular Hypertension Clinical Trials

An Open-Label Study of an Ophthalmic Solution to Reduce Intraocular Pressure in Patients With Ocular Hypertension

Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of topical C-KAD Ophthalmic Solution in reducing intraocular pressure in patients with ocular hypertension.