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Glaucoma, Open-Angle clinical trials

View clinical trials related to Glaucoma, Open-Angle.

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NCT ID: NCT00821002 Completed - Ocular Hypertension Clinical Trials

A Phase 2 Study of Punctal Placement of the Latanoprost Punctal Plug Delivery System (L-PPDS)

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

The study objective is to compare IOP and safety outcomes based on plug placement (upper or lower puncta).

NCT ID: NCT00820300 Completed - Glaucoma Clinical Trials

A Safety Study of the Latanoprost Punctal Plug Delivery System (L-PPDS) 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 if the Punctal Plug Delivery System is safe and effective in controlling intraocular pressure in patients with ocular hypertension or open-angle glaucoma.

NCT ID: NCT00804648 Completed - Ocular Hypertension Clinical Trials

Patient Satisfaction With Timolol in Subjects With Open-Angle Glaucoma or Ocular Hypertension

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

This study compares patient symptoms and anterior segment safety in patients treated with timolol hemihydrate, generic timolol gel forming solution or timolol maleate.

NCT ID: NCT00804102 Completed - Clinical trials for Retinitis Pigmentosa

Transcorneal Electrical Stimulation Therapy for Retinal Disease

Start date: January 2008
Phase: N/A
Study type: Interventional

Transcorneal stimulation may enable neurons to survive degeneration processes via enhanced secretion of neurotrophic substances and direct stimulation of neurons.

NCT ID: NCT00803803 Completed - Open-angle Glaucoma Clinical Trials

Dose, Effects and Characteristics of Pilocarpine

Start date: August 1978
Phase: Phase 4
Study type: Interventional

The purpose of this investigation, in which pilocarpine was given in repeated doses, was to evaluate: Part I - the effects of different concentrations of pilocarpine hydrochloride on intraocular pressure. Part II -the effects on intraocular pressure of glaucomatous patients to pilocarpine 2% when given once, twice and four daily. In addition, we studied various attributes of the eye which may serve as indicators of responsiveness of individual patients to pilocarpine.

NCT ID: NCT00803504 Completed - Clinical trials for Primary Open Angle Glaucoma

Correlation of Optic Disk Morphology and Ocular Perfusion Parameters in Patients With Primary Open Angle Glaucoma

Start date: November 2006
Phase: N/A
Study type: Observational

Glaucoma is one of the most common causes of blindness in the industrialized nations. For a long time glaucoma has been defined as a disease in which high intraocular pressure (IOP) leads to irreversible optic disc damage and subsequent visual field loss. However, recent investigations show that IOP is not the only factor that is involved in the glaucomatous process leading to retinal ganglion cell death. The role of vascular factors in the pathogenesis of glaucoma has recently received much attention based on animal experiments and epidemiological studies. It is, however, assumed that vascular factors do not contribute to same degree in all glaucoma patients. Generally, it is believed that a vascular component is more important in normal tension glaucoma patients and patients with underlying cardiovascular disease. Little is, however, known about a potential association between optic nerve head morphology and ocular perfusion in POAG patients. The current study seeks to gain insight into this association by assessing ocular blood flow parameters with a number of noninvasive technologies.

NCT ID: NCT00803387 Completed - Ocular Hypertension Clinical Trials

Dry Eye and Irritation Comparison of Latanoprost With the Preservative Versus Travoprost Without Preservative

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

Although Benzalkonium chloride (BAC) has been used as a preservative for many years, many studies have demonstrated that prolonged use of topical ocular medications preserved with BAC may exacerbate sequelae associated with ocular surface disease. These effects could lead to the induction of subclinical inflammation,1 reduction of corneal epithelial barrier function, 2, 3 destabilization of the tear film, 4 cataract formation, 5 and an overall higher incidence of patient complaints of dryness and irritation. 4-6 This study will compare the efficacy of travoprost 0.004% without benzalkonium chloride (BAC) to that of the marketed formulation of latanoprost 0.005%with BAC in patients with dryness and irritation and open-angle glaucoma or ocular hypertension. A double blind comparison will be used to assess whether those two different formulations will affect the tear breakup times, corneal staining, and baseline tear secretion tests in patients that are already taking latanoprost regularly with complaints of dryness and irritation. Patients included in the study will be given two bottles, one labeled for their right eye and the other for their left eye. Each pair of bottles will be identical in appearance and randomized with either latanoprost or travoprost and each pair will be assigned a number to aid in future analysis of the final results.

NCT ID: NCT00801437 Completed - Clinical trials for Glaucoma, Open-angle

Non Interventional Study With Primary Open Angle Glaucoma and/or Ocular Hypertension Patients Treated With Xalacom® After Failure of Previous Antiglaucoma Therapy.

Start date: October 2008
Phase:
Study type: Observational

This study is designed to evaluate the safety and tolerability of Xalacom in patients with primary glaucoma

NCT ID: NCT00798759 Completed - Ocular Hypertension Clinical Trials

Examination of Ocular Surface Effects With Administration of Travatan Z and XALATAN

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

The purpose of this study is to compare two ophthalmic solutions in patients with open-angle glaucoma or ocular hypertension.

NCT ID: NCT00781300 Completed - Ocular Hypertension Clinical Trials

Intraocular Pressure With Loteprednol and Dexamethasone

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

The purpose of this study is to compare intraocular pressure (IOP) changes after pterygium surgery among patients using loteprednol and dexamethasone during the postoperative period.