Clinical Trials Logo

Open-Angle Glaucoma clinical trials

View clinical trials related to Open-Angle Glaucoma.

Filter by:

NCT ID: NCT01510145 Completed - Ocular Hypertension Clinical Trials

Efficacy of Changing to TRAVATAN® From Prior Therapy

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study was to assess the efficacy and tolerability of TRAVATAN® solution without BAK (benzalkonium chloride) after changing from prior latanoprost 0.005% ophthalmic solution monotherapy in subjects with open-angle glaucoma or ocular hypertension due to tolerability issues.

NCT ID: NCT01510132 Withdrawn - Ocular Hypertension Clinical Trials

Travacom Post Marketing Surveillance Study

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The purpose of this multi-center, open label, single arm, post-marketing surveillance study is to assess the safety of Travacom in patients with open-angle glaucoma or ocular hypertension who are insufficiently responsive to beta-blockers, prostaglandins, or other intraocular pressure-lowering (IOP) medication and when use of Travacom is considered appropriate.

NCT ID: NCT01493427 Completed - Ocular Hypertension Clinical Trials

Efficacy of Changing to TRAVATAN® From Prior Therapy

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

The purpose of this study was to assess the efficacy and tolerability of TRAVATAN® Solution without benzalkonium chloride (BAK) in patients previously on latanoprost 0.005% or bimatoprost 0.01% ophthalmic solution monotherapy.

NCT ID: NCT01487655 Completed - Open-angle Glaucoma Clinical Trials

Waveform Analysis of the Doppler Curve of Ophthalmic Arteries in Glaucoma Patients

Start date: September 2011
Phase: N/A
Study type: Observational

Color Doppler Imaging (CDI) has been providing information about ocular blood flow over the past decades. This non-invasive procedure based on ultrasound technique has identified increased resistance and decreased systolic blood velocities to exist in the ophthalmic arteries of glaucoma patients. However, existing data has provided very little information regarding the analysis of the Doppler waveform in itself and to whether variables such as early systolic acceleration or systolic/diastolic velocity ratios are of any significance in glaucoma disease. In other medical specialties using CDI technology, such as nephrology or cardiology for instance, this analysis has been part of the normal routine. This information has been used in screening patients for disturbed circulation such as arterial stenosis or providing information regarding prognosis of renal and hepatic transplants have been used for decades now. What is the normal characteristics of the waveform Doppler analysis? To answer this, the investigators will create a normative database using healthy controls. Are there signs of altered stiffness or compliance in the ophthalmic arteries of glaucoma patients? To answer this, the analysis of early acceleration acceleration and detection of an early peak systolic will be done on the Doppler curves of glaucoma patients and compared to the healthy normative database. Are there any difference between the two types of glaucoma [primary open-angle glaucoma (POAG) and normal-tension glaucoma (NTG)]? The investigators will compare the variables of the ophthalmic artery waveform in these two groups. Do any of these Doppler waveform variables have any clinical significance? To answer this, the investigators will search for the existence of any correlation between the waveform data and both functional (visual field testing) and structural (Confocal scanning laser ophthalmoscopy - CSLO) variables of the glaucoma groups.

NCT ID: NCT01485822 Terminated - Open-angle Glaucoma Clinical Trials

A Multicenter Study of the Pigmentation in the Trabecular Meshwork After Two Years of Treatment With TRAVATAN 0.004% Ophthalmic Solution

Start date: July 2004
Phase: Phase 4
Study type: Observational

The purpose of this study was to assess the pigmentation in the trabecular meshwork of patients who had been treated for at least 2 years with TRAVATAN compared with patients without exposure (or less than 1 month) to a prostaglandin analogue (PGA).

NCT ID: NCT01484392 Completed - Open Angle Glaucoma Clinical Trials

Determinants of Compliance With Glaucoma Therapy

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

The purpose of this study is to determine which medical, demographic, and health belief factors are associated with glaucoma therapy compliance.

NCT ID: NCT01464424 Completed - Glaucoma Clinical Trials

Assessment of Intraocular Pressure (IOP) Control in Subjects With Open-Angle Glaucoma or Ocular Hypertension Treated With Travoprost 0.004% (TRAVATAN® Z) or Bimatoprost 0.01% (LUMIGAN®)

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

The purpose of this study was to assess efficacy and tolerability of travoprost 0.004% vs. bimatoprost 0.01% during the after office hour period (4 pm to 8 pm) in subjects with open-angle glaucoma or ocular hypertension after 6 weeks of treatment.

NCT ID: NCT01456390 Completed - Open-Angle Glaucoma Clinical Trials

Open-Angle Glaucoma Subjects With One Prior Trabeculectomy Treated Concurrently With One Suprachoroidal Stent and Two Trabecular Micro-bypass Stents

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

Evaluation in the eyes of subjects with one prior trabeculectomy on one to three ocular hypotensive medications of the intraocular pressure (IOP) lowering effect of two iStent stents in combination with one iStent supra stent and a postoperative prostaglandin.

NCT ID: NCT01455467 Completed - Open-angle Glaucoma Clinical Trials

Open-angle Glaucoma Subjects on One Topical Hypotensive Medication Randomized to Treatment With One or Two Trabecular Micro-bypass Stents in Conjunction With Cataract Surgery

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

Evaluation of intraocular pressure (IOP) lowering effect of one iStent versus two iStents in conjunction with cataract surgery in subjects with primary open-angle glaucoma, washed out of one anti-glaucoma medication prior to stent implantation.

NCT ID: NCT01453855 Completed - Ocular Hypertension Clinical Trials

Travoprost 3-Month Safety and Efficacy Study

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

The purpose of this study was to demonstrate that the intraocular pressure-lowering efficacy of Travoprost 0.003% is equivalent to TRAVATAN® in adult patients with open-angle glaucoma or ocular hypertension.