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Myopia clinical trials

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NCT ID: NCT00347347 Completed - Myopia Clinical Trials

Comparative Study of Cycloplegic Refraction and Subjective Refraction With Fogging in School Age Children

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

A thorough ophthalmic examination of a child must include a refraction and this is often done with cycloplegia. In our study, we aim to determine at which age group a non-cycloplegic refraction technique closely correlates with a cycloplegic refraction and hence, would obviate the need for cycloplegic refraction in our routine clinical practice.

NCT ID: NCT00347204 Completed - Myopia Clinical Trials

Comparison of Acular LS Versus Nevanac for Pain Control in Eyes Undergoing PRK

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

To determine the ability of two topical Nonsteroidal Anti-inflammatory drops (Acular LS & Nevanac) to help control pain following Photorefractive Keratectomy (PRK).

NCT ID: NCT00346593 Completed - Myopia Clinical Trials

Investigation of the Clinical Performance of Silicone Hydrogel Contact Lenses During Continuous Wear

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

The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens during continuous wear (up to 30 nights) over a period of 24 months.

NCT ID: NCT00345228 Completed - Clinical trials for Myopic Macular Haemorrhages

Myopic Macular Haemorrhages

Start date: June 2004
Phase: N/A
Study type: Observational

1. To identify the underlying causes of macular haemorrhages in patients with high myopia 2. In the eyes found to have macular haemorrhages secondary to choroidal neovascularisation, we hope to identify the risk factors for the development of choroidal neovascularisation in high myopia 3. To study the functional outcome of these eyes as assessed by visual acuity 4. To study the morphological outcome of these eyes by clinical assessment (and fundal photography) and fluorescein angiography

NCT ID: NCT00342342 Completed - Glaucoma Clinical Trials

Family Studies of Eye Traits

Start date: December 4, 2002
Phase:
Study type: Observational

This study will examine blood specimens from patients with various eye disorders who previously participated in the Beaver Dam Eye Study to try to identify genes responsible for these disorders. The Beaver Dam study was designed to determine the incidence and causes of age-related eye conditions, including cataract (changes in the lens of the eye that can impair vision); retinopathy (diseases of the retina - the thin layer of tissue that lines the back of the eye); age-related maculopathy (degeneration or atrophy of the macula - the center part of the retina responsible for fine vision); and impaired vision. Findings from this study and others have shown that age-related eye disorders often run in families, indicating a genetic component in their development. All participants in the Beaver Dam study who had family members in the study may be included in the current NHGRI study. The Beaver Dam study included residents of the township of Beaver Dam, Wisconsin, who were between 45 and 84 years of age at enrollment. Participants had thorough eye examinations and blood samples drawn at baseline and 5 and 10 years after the baseline evaluation. Fifteen-year follow-ups will start in 2003. This study will analyze data and blood samples previously collected from Beaver Dam study participants to identify genes related to numerous age-related visual traits. No new participants will be recruited.

NCT ID: NCT00341549 Completed - Myopia Clinical Trials

Family Myopia Study

Start date: April 29, 2002
Phase:
Study type: Observational

This study will try to identify the gene or genes responsible for myopia (nearsightedness) and to examine the relationship between myopia and near work. Myopia is the most common eye disorder in the world, affecting one in four Americans. Several studies indicate that myopia is inherited. The condition tends to cluster in families, so that studying families with this condition may facilitate finding the exact cause. Caucasian Americans and African Americans with myopia who are in general good health may be eligible for this study. People with a family history of myopia through several generations along one parent s side only, and in which more than one sibling has myopia are preferred. People who have severe diseases that involve myopia, such as Stickler s or Marfan syndromes, retinitis pigmentosa or diabetic retinopathy may not participate. Participants will undergo the following tests and procedures: - Eye examination, including refraction - Blood draw for genetic studies and possibly establishment of cell lines (collection of cells grown in the laboratory from an original tissue specimen) for future research - Myopia Family Study Questionnaire and personal medical information questionnaire to provide information about other medical conditions that may influence the development of myopia; the vision status of their spouse and children, parents and siblings, and spouse s parents and siblings - Risk Factor Questionnaire (for Jewish Orthodox community only) to assess the amount of near work activity done in childhood

NCT ID: NCT00335049 Completed - Myopia Clinical Trials

Study of Theories About Myopia Progression (STAMP)

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

At this time, we do not know what causes a child to become more nearsighted (myopic). STAMP will help us better understand nearsightedness in children. Children will be randomly chosen to wear regular glasses (single vision lenses) or no-line bifocal glasses (progressive addition lenses) for the first year of the study. All children will wear regular glasses for the second year of the study. STAMP will compare how the eye changes shape in the two groups to help us understand why children become nearsighted. The two theories of myopia progression that are being evaluated are based on different factors. One theory is based on environmental factors such as extended near work while the other theory is based on genetically coded factors.

NCT ID: NCT00320593 Completed - Myopia Clinical Trials

Correction of Myopia Evaluation Trial 2

COMET2
Start date: April 2005
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine if progressive addition lenses (PALs) versus single vision lenses (SVLs) slow the progression of low myopia in children with poor accommodative responses (i.e., large accommodative lags) and near esophoria.

NCT ID: NCT00317551 Completed - Myopia Clinical Trials

Cambridge Anti-Myopia Trial: Accommodation Training and Aberration Control in Myopia Development

Start date: April 2005
Phase: Phase 2
Study type: Interventional

We have identified focussing problems related to myopia getting worse. Our trial uses optical and orthoptic interventions that correct the focussing problems to see if this retards myopia progression.

NCT ID: NCT00272376 Completed - Myopia Clinical Trials

Clinical and Genetic Studies in Families With Myopia and Related Diseases

Start date: December 21, 2005
Phase:
Study type: Observational

This study will examine the inheritance of myopia in families of various nationalities and ethnic backgrounds to identify gene changes that cause myopia or similar diseases and to better understand these conditions. In patients with myopia, the eye does not focus light accurately on the retina (tissue that lines the back of the eye), so that objects at a distance appear blurry. Myopia may occur alone, with other vision problems such as retinal dislocations, cataract or glaucoma, or with other problems such as joint or skin problems. People with myopia (usually those from families with several affected members) and control subjects with normal vision may be eligible for this study. Each participant undergoes the following procedures: - Blood draw for genetic testing related to the disorders under study - Medical and family history, including drawing a family tree to explore vision problems in the family - Complete eye examination, including refraction (pupil dilation) and visual acuity testing, photographs of the retina and possibly lens, and specialized tests to measure field of vision, color vision and ability to see in the dark