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Pseudoexfoliative Glaucoma clinical trials

View clinical trials related to Pseudoexfoliative Glaucoma.

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NCT ID: NCT02355990 Completed - Clinical trials for Primary Open Angle Glaucoma

Minimally Invasive Micro Sclerostomy First in Man Safety and Preliminary Performance Study

Start date: February 1, 2015
Phase: N/A
Study type: Interventional

The study objective is to demonstrate the safety of Minimally Invasive Micro Sclerostomy (MIMS) device for lowering elevated IOP in patients diagnosed with glaucoma.

NCT ID: NCT02024464 Completed - Clinical trials for Primary Open Angle Glaucoma

Comparing Hydrus Microstent(TM) to the iStent for Lowering IOP in Glaucoma Patients Undergoing Cataract Surgery

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

This clinical trial compares two implantable devices intended to lower the pressure inside the eye of glaucoma patients. One of the two devices will be implanted immediately following cataract surgery and the placement of a posterior chamber intra-ocular lens.

NCT ID: NCT02023242 Completed - Clinical trials for Primary Open Angle Glaucoma

Comparing Effectiveness of the Hydrus Microstent (TM) to Two iStents to Lower IOP in Phakic Eyes

COMPARE
Start date: October 2012
Phase: N/A
Study type: Interventional

This clinical trial compares two implantable devices intended to lower the pressure inside the eye of glaucoma patients.

NCT ID: NCT01767753 Completed - Clinical trials for Primary Open Angle Glaucoma

IOP Fluctuations in Patients With Primary Open-angle Glaucoma, Before and After Selective Laser Trabeculoplasty

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

Selective laser trabeculoplasty (SLT) is an increasingly popular treatment modality in early-to-moderate glaucoma patients. SLT has been suggested to reduce IOP more consistently during the nocturnal period than during the diurnal period in a group of medically-treated patients with primary open angle glaucoma (POAG). At present, there is scarce data on SLT effects on the 24-hour IOP pattern in patients with glaucoma and there is no data on the 24-hour effect of SLT in untreated glaucoma patients. The purpose of this study is to assess the changes of IOP over a 24-hour period in patients with glaucoma undergoing SLT.

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: NCT00441883 Completed - Ocular Hypertension Clinical Trials

Dose-Finding Study Comparing the Safety and Efficacy of Latanoprost to a Novel Treatment for Glaucoma

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

This study will evaluate the safety and efficacy of PF 03187207.

NCT ID: NCT00346931 Terminated - Clinical trials for Primary Open Angle Glaucoma

Phacotrabeculotomy Versus CCI+Phaco in Patients With Borderline Control of Intraocular Pressure

Start date: December 2004
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether combined cataract and glaucoma surgery (phacotrabeculotomy)is more effective in lowering intraocular pressure than cataract surgery alone in patients with borderline control of intraocular pressure.