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Open-Angle Glaucoma clinical trials

View clinical trials related to Open-Angle Glaucoma.

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NCT ID: NCT00471068 Terminated - Ocular Hypertension Clinical Trials

Study of Travatan and Cosopt in Primary Open-Angle Glaucoma or Ocular Hypertension

Start date: March 2007
Phase: Phase 4
Study type: Interventional

To compare the efficacy and safety in patients treated with travoprost versus dorzolamide/timolol maleate combination in patients with open-angle glaucoma or ocular hypertension

NCT ID: NCT00465803 Completed - Ocular Hypertension Clinical Trials

A Phase IIIb Study of DuoTrav to Treat Glaucoma or Ocular Hypertension

Start date: March 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess patient compliance with DuoTrav versus concomitant administration of Timolol 0.5% plus TRAVATAN in patients with open-angle glaucoma or ocular hypertension.

NCT ID: NCT00465621 Completed - Ocular Hypertension Clinical Trials

Dose Response Study of AL-37807 Ophthalmic Solution in Patients With Open-Angle Glaucoma or Ocular Hypertension

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The purpose of thie study is to compare the safety and IOP-lowering efficacy of AL-37807 Ophthalmic Solution 0.05%, 0.1% and 0.2% dosed QD AM to Xalatan dosed QD PM and Vehicle in patients with open-angle glaucoma or ocular hypertension

NCT ID: NCT00457795 Completed - Ocular Hypertension Clinical Trials

24-hour IOP-lowering Effect of Brimonidine 0.1%

Start date: December 2006
Phase: Phase 4
Study type: Interventional

This study will evaluate the efficacy and safety of brimonidine 0.1% three-times daily in patients with glaucoma or ocular hypertension

NCT ID: NCT00451152 Completed - Open-angle Glaucoma Clinical Trials

Safety and Efficacy of Anecortave Acetate in Patients With Open-Angle Glaucoma

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study was to evaluate the safety and intraocular pressure (IOP)-lowering efficacy of anecortave acetate for treatment of elevated IOP in patients with open-angle glaucoma.

NCT ID: NCT00443924 Completed - Ocular Hypertension Clinical Trials

Study of INS115644 Ophthalmic Solution in Subjects With Ocular Hypertension or Glaucoma

Start date: March 2007
Phase: Phase 1
Study type: Interventional

The purpose of this trial is to evaluate the safety and tolerability of INS115644 Ophthalmic Solution in subjects with bilateral ocular hypertension or early primary open angle glaucoma and to investigate the intraocular pressure lowering effects of INS115644 Ophthalmic Solution.

NCT ID: NCT00440336 Recruiting - Open Angle Glaucoma Clinical Trials

Comparison of Efficacy of Two Groups of Glaucoma Drops (Xalatan vs.Cosopt) in Reducing Eye Pressure Following Laser (SLT)Treatment in the Management of Glaucoma.

Start date: October 2006
Phase: N/A
Study type: Interventional

WHAT IS THIS STUDY ABOUT? Glaucoma and ocular hypertension are chronic eye diseases that can damage the optic nerve and lead to vision loss or blindness. The optic nerve acts like an electric cable with over a million wires. This nerve is responsible for carrying images from the eye to the brain. The way glaucoma and ocular hypertension cause blindness depends on many factors, but the most important factor is the increased pressure inside the eye (intraocular pressure). There is no cure for glaucoma or ocular hypertension. However, lowering the pressure inside the eye has been shown to slow the progression of disease. Intraocular pressure can be lowered by glaucoma medication, laser treatment, or surgery. You have open angle glaucoma, pseudoexfoliative glaucoma, or ocular hypertension. Researchers want to find out more about how 2 drugs called Cosopt (dorzolamide hydrochloride and timolol maleate) and Xalatan (latanoprost) can help people with these conditions. Cosopt and Xalatan are both eye drops that are approved by the U.S. Food and Drug Administration (FDA) to reduce intraocular pressure in people with open angle glaucoma and ocular hypertension. The study doctor will do a laser procedure called Selective Laser Trabeculoplasty (SLT) on people in this study to help lower their intraocular pressure. The FDA has approved SLT to treat open angle glaucoma and ocular hypertension. Then the study doctor will ask some participants to use either Cosopt or Xalatan, if their intraocular pressure is still too high 4 to 6 weeks after the SLT procedure. The study doctor wants to see which of the 2 study drugs (Cosopt or Xalatan) is better at reducing intraocular pressure after SLT. It is planned that about 30 people with glaucoma or ocular hypertension who are at least 18 years old will be in this study. Out of the participants whose intraocular pressure is still too high after SLT, half will use Cosopt and half will use Xalatan. You do not have to be in this study to have SLT or to use Cosopt or Xalatan.

NCT ID: NCT00430287 Completed - Open Angle Glaucoma Clinical Trials

Does the Optic Disc Grading Done Visually by Your Doctor Agree With Optic Nerve Testing Which is Done by Machines?

Start date: March 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine how well the DDLS (Disc Damage Likelihood Scale) (which is a method used by the eye doctor to evaluate how healthy the optic nerve is) measures up to the standard glaucoma tests: OCT (Optical Coherence Tomography), the HRT (Heidelberg Retinal Tomography) and the HVF (Humphrey Visual Field).

NCT ID: NCT00397241 Completed - Open-angle Glaucoma Clinical Trials

24-hour Study of Dorzolamide/Timolol and Latanoprost/Timolol Fixed Combinations

Start date: September 2006
Phase: Phase 4
Study type: Interventional

The primary objective of this crossover trial is to compare the 3-month mean 24-hour intraocular pressure (IOP) control and safety of dorzolamide/timolol fixed combination (DTFC) given twice daily, versus latanoprost/timolol fixed combination (LTFC) given in the evening and placebo given in the morning, versus adjunctive therapy with DTFC given twice daily and latanoprost 0.005% given once in the evening in open-angle glaucoma patients who are insufficiently controlled with latanoprost monotherapy.

NCT ID: NCT00372931 Completed - Ocular Hypertension Clinical Trials

A Phase II Study of AL-37807 to Treat Open-Angle Glaucoma or Ocular Hypertension

Start date: May 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether AL-37807 is safe and effective in treating patients with open-angle glaucoma or ocular hypertension