Clinical Trials Logo

Glaucoma clinical trials

View clinical trials related to Glaucoma.

Filter by:

NCT ID: NCT00570362 Completed - Clinical trials for Normal Tension Glaucoma

Systemic Glutathione Level in Normal Tension Glaucoma

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

The purpose of this study is to evaluate whether systemic glutathione level is decreased in patients with normal tension glaucoma.

NCT ID: NCT00567788 Active, not recruiting - Clinical trials for Glaucoma, Angle-Closure

Comparison of Bimatoprost and Latanoprost in Patients With Chronic Angle-Closure Glaucoma: A Randomized Cross-Over Study

Start date: July 2006
Phase: N/A
Study type: Interventional

This is a randomized observer-masked cross-over study to compare the intraocular pressure (IOP) reducing effect of latanoprost with bimatoprost in subjects with chronic angle closure glaucoma (CACG) with raised IOP. Study subjects will be randomized to receive either latanoprost once daily or bimatoprost once daily for 6 weeks, after which they will be crossed over to the other medication for another 6 weeks. The IOP-reducing effect of the medications will be assessed by the reduction in IOP after each medication compared to baseline. The study will be carried out in at least 2 Singapore hospitals.

NCT ID: NCT00567411 Recruiting - Glaucoma Clinical Trials

Comparison of the Alpha-2 Agonists for Prevention of Intraocular Pressure Elevation After Selective Laser Trabeculoplasty

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

The purpose of the study is to compare the safety and efficacy of two drops used to lower eye pressure when given prior to a glaucoma laser procedure.

NCT ID: NCT00559234 Completed - Cataract Clinical Trials

Potential Research Participants for Future Studies of Inherited Eye Diseases

Start date: November 9, 2007
Phase: N/A
Study type: Observational

This study will evaluate potential candidates for future clinical research studies related to diagnosed or undiagnosed genetic eye disorders or diseases. It will not test any new treatments, but it may arrange for standard treatments for existing eye disorders. The purpose of the study is to train eye doctors and medical researchers at the National Institutes of Health in appropriate methods and procedures for treating patients with genetic eye diseases, and to expand the pool of possible participants for future research studies and trials on eye health. Volunteers for this study may be adults and minor children who have been diagnosed with or are at risk for having a genetic eye disease. Candidates may not have any other medical conditions that would interfere with the researchers' ability to perform the examinations and procedures required for this study. Participants will give a complete medical and family history and undergo a series of tests and procedures as part of this research study. The procedures include a full eye examination and vision testing, electrooculography and an electroretinogram to examine the function of the retina, and flourescein angiography to provide information on the flow of blood in the participant's eyes. Participants will provide research material for further studies by giving a blood sample to be held for genetic testing and analysis, and adult participants will also undergo a skin biopsy to provide cell tissue for additional research material. At each clinic visit, participants will receive treatment for their genetic eye disease as needed, including medications or surgical procedures. Participants may remain a part of this study for up to three years.

NCT ID: NCT00557232 Completed - Glaucoma Clinical Trials

Intraocular Bevacizumab (Avastin) for Rubeosis Iridis

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

Bevacizumab (Avastin®, Roche, Rio de Janeiro, Brazil) is an anti-VEGF recombinant humanized monoclonal IgG1 antibody used to treat colorectal cancers. Bevacizumab may have a role in treating ocular disorders involving fibrovascular proliferation. To determine whether intraocular bevacizumab decreases rubeosis iridis in patients with neovascular glaucoma.

NCT ID: NCT00556114 Completed - Glaucoma Clinical Trials

A Pilot Study of Functional Optical Coherence Tomography for Ocular Imaging

Start date: January 2007
Phase:
Study type: Observational

Growing evidence shows that altered blood flow plays a major role in many vision-threatening diseases including glaucoma, diabetic retinopathy, age-related macular degeneration, Central Retinal Vein Occlusion, and Branch Retinal Vein Occlusion. Optical coherence tomography, an established imaging technique use for eye exam in clinical ophthalmology, provides high-resolution cross sectional images of the retina and has increased our ability to understand many eye diseases.

NCT ID: NCT00554411 Completed - Glaucoma Clinical Trials

Assessing Ocular Surface Changes After Changing Glaucoma Medications

Start date: November 2007
Phase: N/A
Study type: Observational

Hypothesis: Changing to Travatan Z therapy increases the tear film break up time of subjects on Xalatan therapy presenting with ocular surface disease.

NCT ID: NCT00551902 Withdrawn - Glaucoma Clinical Trials

Effect of an Anterior Chamber Infusion System on Trabeculectomy Outcomes

Start date: September 2007
Phase: Phase 1
Study type: Interventional

In the treatment of glaucoma, trabeculectomy surgery provides a drainage system for the eye and allows for the lowering of the pressure inside the eye. The flow through the surgically created fistula determines the intraocular pressure. Titrating suture tightness is important to achieving the desired post-operative intraocular pressure. This process is not straightforward and intraocular pressures are often too high or too low post-operatively.

NCT ID: NCT00551395 Terminated - Glaucoma Clinical Trials

Timing of Treatment Completion in Staged Selective Laser Trabeculoplasty (SLT): Early vs. Late Completion

Start date: September 2007
Phase: Phase 3
Study type: Interventional

This study will evaluate the effect of the timing of treatment completion in two-staged selective laser trabeculoplasty therapy on intraocular pressure lowering effect.

NCT ID: NCT00546286 Completed - Glaucoma Clinical Trials

A Study to Evaluate the Effectiveness of Cosopt® as First Line Therapy (MK-0507A-153)

Start date: May 31, 2006
Phase: Phase 3
Study type: Interventional

Evaluate the effectiveness of dorzolamide-timolol (Cosopt®) as first line therapy in reducing intraocular pressure in patients with untreated Open angle glaucoma (OAG) or Ocular hypertension (OH).