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Glaucoma clinical trials

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NCT ID: NCT00760539 Completed - Ocular Hypertension Clinical Trials

Safety and Efficacy of Travoprost/Timolol BAC-free

Start date: June 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate equivalent safety and IOP-lowering effectiveness of two Travoprost/Timolol combination products in patients diagnosed with open-angle glaucoma or ocular hypertension. This global study will be conducted in the US (C-07-64, NCT00672997) and Japan (C-08-08, NCT00760539).

NCT ID: NCT00760240 Completed - Glaucoma Clinical Trials

Ability of Patients With Low Vision to Properly Instill Eye Drops

Start date: September 2008
Phase: N/A
Study type: Observational

The investigators are interested in seeing how people with low vision (decreased visual acuity or restricted visual fields) instill eye drops into their own eyes. The investigators hypothesis is that this population will have more difficulty with self-instillation of drops than a better-seeing population. The investigators aim to explore whatever factors may be involved in preventing this population from getting prescribed eyedrops into their eyes, whether it is more related to visual field or visual acuity.

NCT ID: NCT00759941 Completed - Glaucoma Clinical Trials

A Comparison of Azopt Versus Placebo Added to Xalatan in Patients With Elevated Intraocular Pressure (IOP) on a Prostaglandin

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

The purpose of this study was to assess the efficacy of adding Azopt dosed three times a day to Xalatan as compared to that of adding placebo to Xalatan in patients with elevated intraocular pressure.

NCT ID: NCT00759239 Completed - Ocular Hypertension Clinical Trials

Phase IV Randomised Double-masked Clinical Trial: Assessing Morning Versus Evening Dosing of a Fixed Dose Combination of Travoprost 0.004% / Timolol Maleate 0.5% in Patients With Primary Open-angle Glaucoma or Ocular Hypertension

Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the IOP-lowering efficacy of a combination of Travoprost / Timolol maleate, dosed in the morning or in the evening, in patients with open-angle glaucoma or ocular hypertension, who have an insufficiently controlled IOP (mmHg), and are using prostaglandin analogue monotherapy.

NCT ID: NCT00757835 Completed - Glaucoma Clinical Trials

24-hr IOP With Travoprost/Timolol Compared With Latanoprost/Timolol in XFG

Start date: May 2008
Phase: Phase 4
Study type: Interventional

A crossover, randomized, single-masked study which compares the short-term (3 months) 24-hour IOP control and safety of travoprost/timolol fixed combination given once in the evening, versus that of latanoprost/timolol fixed combination given once in the evening in patients with exfoliative glaucoma. The primary objective of this trial is to compare the quality of 24-hour IOP control after 3 months of chronic therapy with these two medications.

NCT ID: NCT00756184 Completed - Glaucoma Clinical Trials

Value of an Intervention to Enhance Adherence in Glaucoma Patients

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

A one-year, randomized, attention placebo-controlled trial investigating the value of comprehensive adherence specific interventions, over the course of one year, to enhance adherence in both (a) newly diagnosed open-angle glaucoma, or ocular hypertension patients, naive to medical therapy and (b) those who have failed monotherapy with any prostaglandin analogue (and are therefore candidates for adjunctive therapy) who then are randomized to receive only travoprost monotherapy. Subjects will be randomized to two different interventions involving direct physician education, each of which will take approximately the same amount of physician time: The first will be intensive adherence education that will continue throughout the year. The second will be intensive eye care education, but without any direct adherence education. All patients participating in the study will be monitored for adherence by the TDA. The study will demonstrate for the first time the role of adherence-specific training in improving patient adherence and will validate the TDA in monitoring and improving adherence in glaucoma. This will correlate with prior work that has documented that greater adherence is associated with marked improvement in intraocular pressure (IOP) control. A second goal will be seeing whether improving adherence will change the course of glaucoma therapy by making therapeutic failures into therapeutic successes by reducing the need for adjunctive therapy using only monotherapy with travoprost.

NCT ID: NCT00753168 Completed - Ocular Hypertension Clinical Trials

Phase 1-2 Evaluation of OT-730 Eye Drops in Reducing the Intraocular Pressure in Patients With Ocular Hypertension or Open-Angle Glaucoma

Start date: September 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and potential efficacy of a new drug, OT-730 ophthalmic solution (eye drops), in reducing intraocular pressure in the eyes of patients with open angle glaucoma or ocular hypertension. It will be compared with commercial timolol and placebo eye drops.

NCT ID: NCT00751127 Completed - Glaucoma Clinical Trials

A 6 Month Study Comparing Latanoprost With Timolol in Patients With Open Angle Glaucoma or Ocular Hypertension

Start date: January 1993
Phase: Phase 3
Study type: Interventional

PhXA41 is not inferior to timolol

NCT ID: NCT00751062 Completed - Ocular Hypertension Clinical Trials

A Study of Open Angle Glaucoma or Ocular Hypertension in Patients Within Scandinavia

Start date: November 1992
Phase: Phase 3
Study type: Interventional

PhXA41 is not inferior to timolol in reducing intra-ocular pressure

NCT ID: NCT00751049 Completed - Ocular Hypertension Clinical Trials

A Study of Open Angle Glaucoma or Ocular Hypertension in Patients Within the United Kingdom

Start date: December 1992
Phase: Phase 3
Study type: Interventional

Study PhXA41 for its non-inferiority compared with timolol in lowering intra-ocular pressure