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Glaucoma clinical trials

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NCT ID: NCT00626782 Completed - Glaucoma Clinical Trials

Lucentis Versus Mitomycin C During Glaucoma Surgery

Start date: January 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Does a new add on (or adjunctive) therapy used in glaucoma surgery improve the success of trabeculectomy? Ranibizumab may offer benefit similar to mitomycin C in preventing epi-scleral fibrosis while avoiding the well known complications of mytomycin C which include late bleb leaks, hypotony and infection.

NCT ID: NCT00626067 Completed - Glaucoma Clinical Trials

Study of Patient Use and Perception of the Travatan Dosing Aid

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

The primary objective of this study is to determine the opinions of patients who are given the Travatan Compliance Monitoring Dispenser to use to dispense their Travatan glaucoma drops.

NCT ID: NCT00621335 Completed - Ocular Hypertension Clinical Trials

A Investigator Masked Parallel Comparison of Tolerability of Combigan and Cosopt

CICOM1010
Start date: March 2007
Phase: N/A
Study type: Observational

The objective of this research study is to compare the tolerability and effectiveness of Combigan(brimonidine tartrate/timolol maleate) and Cosopt (dorzolamide hydrochloride)in the treatment of open angle glaucoma or ocular hypertension.

NCT ID: NCT00620256 Completed - Ocular Hypertension Clinical Trials

Adjunctive Study of AL-37807 Ophthalmic Suspension

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

The purpose of the study is to compare the safety and intraocular pressure-lowering efficacy of AL-37807 ophthalmic suspension vs. Timolol gel forming solution vs. AL-37807 vehicle, all dosed concomitantly with Xalatan, in patients with open-angle glaucoma or ocular hypertension.

NCT ID: NCT00607685 Completed - Glaucoma Clinical Trials

5FU vs 5FU With Viscoelastic Formulation for the Prevention of Scarring Post-trabeculectomy

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

Trabeculectomy is the most effective method of lowering intraocular pressure in glaucoma that is not well controlled with drop medication. The post-operative wound healing response remains the major barrier in surgical success. Scar tissue formation results in occlusion of the surgical drainage site created. As a consequence, the intraocular pressure rises once again. The current use of anti-scarring agents such as 5 Fluorouracil (5FU), is a well established method employed by ophthalmologists to clinically reduce the postoperative scarring response. However, in patients with a high risk of bleb failure, repeated subconjunctival injections of 5FU following bleb needling is often required resulting in increased clinical load and patient inconvenience. A slow release formulation of 5FU would be of benefit by releasing the 5FU into the subconjunctival space over an extended period thereby providing a prolonged therapeutic effect. In addition, hyaluronic acid is known to possess antifibrotic properties and from its gel-like physical state, would potentially act as a physical tissue spacer that may further limit active subconjunctival scarring at the site where it is injected. We hypothesise that injecting a mixture of 5FU with hyaluronic acid would give better outcomes than injecting 5FU alone. The aim of this study is to determine whether bleb needling with subconjunctival injection of Viscoelastic/5FU formulation is an effective method for prolonged drug delivery in preventing the post-operative scarring response. This will be a prospective case-controlled study involving patients who have already undergone trabeculectomy and who require bleb needling and subconjunctival 5FU injections.

NCT ID: NCT00603005 Completed - Glaucoma Clinical Trials

Adherence Improvement in Glaucoma Patients

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

The purpose of this study is to study the effect on intraocular pressure in glaucoma patients using the TravAlert dosing aid with or without the Eyot drop guider and with or without additional patient education.

NCT ID: NCT00596791 Completed - Ocular Hypertension Clinical Trials

Ocular Signs and Symptoms in Glaucoma Patients Switched From Latanoprost 0.005% to Preservative Free Tafluprost Eye Drops

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

The purpose of this study is to investigate if changes in ocular signs and symptoms occur in patients with ocular hypertension or glaucoma when they switch from latanoprost 0.005% (Xalatan) to preservative free Tafluprost eye drops.

NCT ID: NCT00595855 Completed - Glaucoma Clinical Trials

A Comparison Between Deep Sclerectomy and Trabeculectomy

Start date: October 1997
Phase: N/A
Study type: Interventional

Patients affected by medically uncontrolled open angle glaucoma will be randomised to either a non penetrating procedure (deep sclerectomy) or conventional trabeculectomy. The longterm efficacy (i.e. IOP w/out therapy) and safety (i.e. visual acuity, visual field stability and co-morbidities) will be evaluated.

NCT ID: NCT00595101 Completed - Ocular Hypertension Clinical Trials

A Phase 2, Dose Finding Study of PF-03187207 in Patients With Primary Open Angle Glaucoma or Ocular Hypertension.

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

To investigate dose response, safety and efficacy of PF-03187207 in patients with primary open-angle glaucoma or ocular hypertension

NCT ID: NCT00576342 Completed - Glaucoma Clinical Trials

Patient Preference Study

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

In this randomized crossover study, patients will receive a single drop of two test articles and assess comfort.