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Glaucoma clinical trials

View clinical trials related to Glaucoma.

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NCT ID: NCT01742819 Active, not recruiting - Clinical trials for Primary Open Angle Glaucoma

Advanced Glaucoma Progression Study

AGPS
Start date: May 2012
Phase:
Study type: Observational

Glaucoma is one of the leading causes of blindness in the world. The key to prevention of visual loss from glaucoma is early detection of the disease or its progression and timely treatment. The proposed study will investigate the role of various tests in improving detection of disease progression in advanced glaucoma. Evaluation of the peripheral field of vision (visual field examination) remains the current standard for detection of progression in glaucoma. However, there is a lot of variability or inconsistency in eyes with advanced glaucoma, which could make it difficult to detect worsening of glaucoma with visual fields. The optic nerve demonstrates significant damage in such eyes and hence oftentimes repeat imaging of the optic nerve head is not helpful for detection of change. Therefore, imaging of the central retina (the innermost sensitive tissue lining the inside of the eye), called macula, has been proposed to supplant imaging of the nerve in eyes with severe glaucoma. The macula aids in detailed central vision. Since the macular retinal neural cells are the last ones to be affected in glaucoma, measurement of macular retinal thickness could provide significant information with regard to the course of glaucoma. In the proposed study, glaucoma patients will be tested and followed with various measurements done with newer versions of optical coherence tomography (OCT) imaging and visual field machines. The patients will undergo repeat imaging and visual field testing every 6 months over the course of 5 years. Rates of change will be estimated. We will explore if changes in various outcome measures derived from imaging are correlated with the corresponding visual field changes in glaucoma, and whether the former can be used as an alternative method for detecting simultaneous or subsequent glaucoma progression. The hypothesis for this proposed research is that macular OCT parameters are valid structural measures that can be used especially in advanced disease to follow the course of glaucoma.

NCT ID: NCT01742104 Completed - Clinical trials for Primary Open-angle Glaucoma

Multicentric Observational Study on Quality of Life in Glaucoma

Start date: March 2012
Phase: N/A
Study type: Observational

The study aims to evaluate the quality of life (QoL) of patients affected by Primary Open-Angle Glaucoma (POAG), using 2 QoL questionnaires: 1. Glaucoma Symptom Scale (GSS) and 2. National Eye Institute Visual Function Questionnaire (NEI-VFQ -25). The study will be conducted on patients with well known diagnosis of POAG (transversal phase) and on patients with first diagnosis of POAG (longitudinal phase).

NCT ID: NCT01741961 Completed - Glaucoma Clinical Trials

Long Term Outcome After Ahmed Glaucoma Valve

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

Long term results after Ahmed glaucoma valve implantation for uncontrolled glaucoma are retrospectively examined.

NCT ID: NCT01739244 Completed - Ocular Hypertension Clinical Trials

Dose Finding Clinical Trial With SYL040012 to Evaluate the Tolerability and Effect on Intraocular Pressure in Subjects With Ocular Hypertension or Open Angle Glaucoma

Start date: July 2012
Phase: Phase 2
Study type: Interventional

The aim of this dose-finding clinical trial is to evaluate the systemic tolerability, local tolerability and intraocular pressure lowering effect of three different doses of SYL040012 in subjects with ocular hypertension or open-angle glaucoma.

NCT ID: NCT01737853 Completed - Clinical trials for Glaucoma Primary Open Angle

Comparison of Efficacy & Tolerability Between Ganfort vs Krytantek in Mexican Patients With Primary Open-Angle Glaucoma (POAG) or Ocular Hypertension (OHT)

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

The objective of this phase IV clinical multi-center trial will be to compare the efficacy and safety of Ganforti® versus Krytantek®, using a cross-over design during a six month period (including a one-month wash-in period) in POAG and OH patients.

NCT ID: NCT01735214 Completed - Ocular Hypertension Clinical Trials

An Observational Study of Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT) Who Switched IOP-lowering Treatments

Start date: March 7, 2013
Phase:
Study type: Observational

This study is a prospective, observational study of changing from any IOP-lowering treatment to a prostaglandin analogue-containing IOP-lowering medication for patients with Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT). The decision to change medications lies with the physician according to their standard practice.

NCT ID: NCT01733550 Not yet recruiting - Glaucoma Clinical Trials

ICare Self-tonometry - A Head-to-head Comparison to the Gold Standard Goldmann Tonometer

Start date: November 2012
Phase: N/A
Study type: Observational

The purpose of this study is to compare glaucoma patients' own I Care measurements by the standard Goldmann applanation tonometer intraocular pressure (IOP) measurements.

NCT ID: NCT01731002 Completed - Ocular Hypertension Clinical Trials

Study Comparing the Safety and Efficacy of AR-13324 to Latanoprost in Patients With Elevated Intraocular Pressure

Start date: November 2012
Phase: Phase 2
Study type: Interventional

Double-masked, randomized, multi-center, dose-response, active-controlled parallel-comparison of AR-13324 to latanoprost

NCT ID: NCT01726569 Withdrawn - Glaucoma Clinical Trials

Post-operative Satisfaction With Glaucoma Surgery Trial

Start date: December 2012
Phase: N/A
Study type: Interventional

1. Investigate degree of postoperative satisfaction in county level hospital glaucoma patients. 2. Investigate the effect of educational intervention affect the degree of satisfaction in glaucoma patients. 3. Investigate the effect factors of postoperative satisfaction.

NCT ID: NCT01726543 Recruiting - Cataract Clinical Trials

Safety and Efficacy of Canaloplasty and Non-penetrating Deep Sclerectomy With Phacoemulsification to Treat Glaucoma and Cataract

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

It is a comparative study of Safety and Efficacy of Canaloplasty and Non-penetrating Deep Sclerectomy Combined With Phacoemulsification to Treat Glaucoma and Cataract. It is a Randomised, Prospective Study.