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Myopia clinical trials

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NCT ID: NCT00263471 Unknown status - Myopia Clinical Trials

Myopia Progression and the Effect of 7-Methylxanthine

Start date: October 2003
Phase: Phase 2
Study type: Interventional

7-methylxanthine has been shown to increase the concentration and thickness of collagen fibrils in rabbit sclera. Deficient collagen in the sclera may be the cause of progression of childhood myopia. The study hypothesis is that treatment with 7-methylxanthine will stabilize the sclera and prevent further progression of myopia.

NCT ID: NCT00241280 Completed - Myopia Clinical Trials

Study Intended to Evaluate the Safety and Effectiveness of a Johnson & Johnson Vision Care Inc, (JJVCI) Contact Lens for Use on an Extended-wear Basis for up to 7 Days (6 Nights).

Start date: September 2005
Phase: N/A
Study type: Interventional

Study in the US intended to evaluate the safety and effectiveness of a Johnson & Johnson Vision Care Inc, (JJVCI) contact lens for use on an extended-wear basis for up to 7 days (6 nights).

NCT ID: NCT00221897 Recruiting - Myopia Clinical Trials

Diagnostic Innovations in Glaucoma Study

DIGS
Start date: April 1995
Phase:
Study type: Observational

The overarching goal of our research study is to evaluate changes in visual function and optic nerve topography (the structure of the back of the eye) in patients with glaucoma (increased susceptibility to pressure inside the eye that can cause loss of vision) or those with an increased risk of developing the disease. The purpose of this study is to determine the best methods for detecting the presence or progression (worsening over time) of glaucoma in patients with and without myopia and its effects on daily and visual function and quality of life. With several sources of NIH and foundation funding over the last twenty years we have designed a robust research protocol to address the most challenging aspects of glaucoma management. The most recent focus of this research is 1) to improve our ability to detect open angle glaucoma in individuals with myopia and in individuals of European and African descent, 2) to determine whether monitoring of the retinal vasculature with new optical imaging instruments can improve glaucoma management and elucidate the pathophysiology of the disease, and 3) to differentiate between age-related changes and glaucomatous progression. The grants supporting this project include 3 NIH funded studies, 1) the University of California, San Diego UCSD -based "Diagnostic Innovations in Glaucoma Study" (DIGS funded since 1995): 2) the "African Descent and Glaucoma Evaluation Study" (ADAGES funded since 2002), 3) the Brightfocus Foundation National Glaucoma Research Program and 4) the UCSD-based "Diagnosis and Monitoring of Glaucoma with Optical Coherence Tomography Angiography" (funded since 2018). The ADAGES is a multi-center study with data collection also conducted at 2 other academic sites, the University of Alabama at Birmingham, and Columbia University. Enrolled healthy participants, glaucoma suspects and glaucoma patients are generally asked to return for two or more visits a year for several years. We then analyze whether the glaucoma patients are progressing and what factors influence their glaucoma status compared to healthy subjects and individuals suspected of having glaucoma.

NCT ID: NCT00214487 Completed - Myopia Clinical Trials

Bifocal Soft Contact Lenses and Their Effect on Myopia Progression in Children and Adolescents.

Start date: October 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether bifocal soft contact lenses are effective in controlling the progression of myopia in children and adolescents that exhibit a tendency to excessively cross their eyes while reading (esophoria or eso fixation disparity). Several studies have demonstrated that bifocal or progressive multifocal spectacles are effective in slowing the progression of myopia in children either with near point esophoria and/or with inadequate focusing at near. A prominent theory for one cause of myopia progression is that poorly focused images on the back of the eye (retina) cause the eye to lengthen, causing an increase in myopia. Bifocal contact lenses may reduce this retinal defocus, reducing the stimulus to eye elongation, and thus may reduce myopia progression.

NCT ID: NCT00172952 Recruiting - Myopia Clinical Trials

The Role of SNP of ECM and MMP on the Development of Pathological High Myopia

Start date: June 2005
Phase: N/A
Study type: Observational

To study the clinical characteristics and inheritance of pathological myopia in Taiwanese patients.

NCT ID: NCT00172913 Recruiting - Myopia Clinical Trials

Aberration-Free Refraction Correction

Start date: June 2005
Phase: N/A
Study type: Observational

In the interest of improving visual quality after LASIK we have designed a multifaceted study to test the theoretical, physical, biomechanical and functional effects of commercial and independently designed aspherical ablation profiles.

NCT ID: NCT00155753 Recruiting - Pathological Myopia Clinical Trials

Genomewide Screening of Pathological Myopia

Start date: August 2002
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the possible candidate gene of pathological myopia

NCT ID: NCT00009529 Completed - Myopia Clinical Trials

The Contact Lens and Myopia Progression (CLAMP) Study

Start date: n/a
Phase: N/A
Study type: Observational

To examine the effects of rigid gas permeable contact lenses on the progression of myopia (nearsightedness) in children To determine what changes in the eyes cause certain eyes to progress in nearsightedness more slowly

NCT ID: NCT00000169 Recruiting - Myopia Clinical Trials

The Collaborative Longitudinal Evaluation of Ethnicity and Refractive Error (CLEERE) Study

Start date: April 1999
Phase: N/A
Study type: Observational

To compare and contrast normal eye growth, ocular component development, and refractive error development in Hispanic, African-American, and Asian schoolchildren with what happens in Caucasian children from the Orinda Longitudinal Study of Myopia. To investigate risk factors for the development of myopia. To conduct DNA-based studies on nearsighted children and their families.

NCT ID: NCT00000129 Completed - Myopia Clinical Trials

Prospective Evaluation of Radial Keratotomy (PERK) Study

Start date: April 1981
Phase: Phase 3
Study type: Interventional

To determine whether radial keratotomy is effective in reducing myopia. To detect complications of the surgery. To discover patient characteristics and surgical factors affecting the results. To determine the long-term safety and efficacy of the procedure.