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Glaucoma clinical trials

View clinical trials related to Glaucoma.

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NCT ID: NCT01444040 Completed - Open-angle Glaucoma Clinical Trials

Subjects With Open-angle Glaucoma, Pseudoexfoliative Glaucoma, or Ocular Hypertension Naïve to Medical and Surgical Therapy, Treated With Two Trabecular Micro-bypass Stents (iStent Inject) or Travoprost

Start date: September 2011
Phase: Phase 4
Study type: Interventional

Evaluation of the intraocular pressure (IOP) lowering effect of two iStent inject devices versus medical therapy in eyes of subjects with primary open-angle glaucoma, pseudoexfoliative glaucoma, or ocular hypertension naïve to medical and surgical therapy.

NCT ID: NCT01443988 Completed - Open-angle Glaucoma Clinical Trials

Subjects With Open-angle Glaucoma, Pseudoexfoliative Glaucoma, or Ocular Hypertension Naïve to Medical and Surgical Therapy, Treated With Two Trabecular Micro-bypass Stents (iStent)or Travoprost

Start date: September 2011
Phase: Phase 4
Study type: Interventional

Evaluation of the intraocular pressure (IOP) lowering effect of two iStent devices versus medical therapy in eyes of subjects with primary open-angle glaucoma, pseudoexfoliative glaucoma, or ocular hypertension naïve to medical and surgical therapy.

NCT ID: NCT01442896 Completed - Clinical trials for Primary Open Angle Glaucoma

STudy to Assess Rapid Disease Progression by Clinical and Genetic Factors In Glaucoma patientS That Are High Risk

STARFISH
Start date: September 1, 2011
Phase:
Study type: Observational

The purpose of this study is to perform exploratory analyses to evaluate rates of functional and structural change in glaucoma, to identify predictors of rapid progression in patients with glaucoma and to identify possible genetic factors and biomarkers associated with the disease.

NCT ID: NCT01440751 Completed - Glaucoma Clinical Trials

Comparative Study of Ologen Collagen Matrix Versus Mitomycin-C in Glaucoma Filtering Surgery

MCToCM
Start date: September 2011
Phase: Phase 4
Study type: Interventional

The objective of this prospective randomised study is to compare the efficacy and safety of ologen CM (Collagen matrix) and Mitomycin-C (MMC) as adjuncts to filtration surgery in uncontrolled treated glaucoma cases, the efficacy being the primary objective and the safety being the secondary.

NCT ID: NCT01433900 Recruiting - Glaucoma Clinical Trials

Switching From Preserved to Preserved-free Treatments for Glaucoma.

Start date: May 2012
Phase: Phase 3
Study type: Interventional

A 1-year prospective, randomized, investigator-masked trial comparing the confocal and clinical effects of treatment with unpreserved prostaglandins (tafluprost) versus preserved prostaglandins (latanoprost) in newly-diagnosed glaucoma patients.

NCT ID: NCT01426867 Completed - Ocular Hypertension Clinical Trials

A Comfort Study of Brinzolamide 1% / Brimonidine 0.2% Fixed Combination, Brinzolamide 1% and Brimonidine 0.2%

Start date: September 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study was to describe the ocular discomfort immediately upon instillation of Brinzolamide 1%/Brimonidine 0.2% Tartrate Ophthalmic Suspension, Brinzolamide 1% Ophthalmic Suspension, and Brimonidine Tartrate 0.2% Ophthalmic Solution in subjects with open-angle glaucoma and/or ocular hypertension.

NCT ID: NCT01426464 Not yet recruiting - Glaucoma Clinical Trials

Intraocular Pressure (IOP) Lowering Efficacy of Transdermal Latanoprost Therapy

Start date: September 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness in lowering intraocular pressure (IOP) utilizing an experimental lotion containing 0.005% Latanoprost that is applied to the outside of one eyelid.

NCT ID: NCT01426113 Terminated - Glaucoma Clinical Trials

A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paediatric Patients With Glaucoma

Start date: September 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of a new formulation of bimatoprost ophthalmic solution compared to timolol ophthalmic solution in the treatment of paediatric patients with glaucoma.

NCT ID: NCT01417689 Recruiting - Glaucoma Clinical Trials

Eyedrop Instillation Technique

Start date: August 2011
Phase: N/A
Study type: Interventional

Eye drop instillation is a problem from glaucoma patients. Studies reveal that 30-50% of glaucoma patients have problems instilling their eyedrops. These problems include not hitting the eye, spending many drops to get a single successful instillation and bottle contamination. The present study will evaluate the effect of encouraging patients to put their eyedrops using one of 2 techniques, randomly assigned, to determine which is more successful at instilling the eye drop into the eye while spending the least amount of drug. In one of the techniques the patient instills the eye drop with their eyes open in the inferior cul de sac. In the other technique the patient instills the eye drop with the eyes closed near the inner canthal region. Patients will be randomized to encouragement to use the drops with either of the techniques. Encouragement will take place over a visit where they will be subjected to: - Baseline evaluation of eye drop instillation using their usual technique. - Short (2-5 minute) educational session session for the assigned technique. - Followup evaluation immediately after the educational session.

NCT ID: NCT01416415 Terminated - Clinical trials for Glaucoma, Open-Angle

Glaucoma Eye Drop Instillation: Impact of Education

Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether an educational intervention will have a positive effect on patients' ability to properly administer eye drops. The investigators predict that the educational intervention will have a positive impact on the efficacy, safety, and efficiency with which patients administer their eye drops.