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Myopia clinical trials

View clinical trials related to Myopia.

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NCT ID: NCT00349882 Completed - Myopia Clinical Trials

Effects of Contact Lens Care Regimens on the Corneal Epithelium

Start date: June 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the performance of two different contact lens care solutions, specifically their affects on the front surface of the eye.

NCT ID: NCT00349856 Completed - Myopia Clinical Trials

Dispensing Overnight Study in Lenses

Start date: January 2005
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the fit and performance of an investigational soft contact lens in comparison with a currently marketed lens. Both lenses will be worn on a continuous wear basis, which means the lenses will be worn while sleeping.

NCT ID: NCT00349843 Completed - Myopia Clinical Trials

Investigation of Multi-Purpose Solution-Based Corneal Staining and Ocular Comfort

Start date: June 2005
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to compare subjective ocular symptoms and corneal staining over time in a group of individuals who wear soft contact lenses on a daily wear basis, whilst they sequentially use two different contact lens care regimens.

NCT ID: NCT00348218 Completed - Myopia Clinical Trials

Pilot Study of Neurovision to Improve Vision and Slow Myopia Progression in Children With Myopia

Start date: June 2006
Phase: Phase 1
Study type: Interventional

This is a pilot study to assess the effectiveness of Neurovision treatment in the improvement of vision in children being under-corrected and to assess the effectiveness of Neurovision treatment in slowing down myopia progression in children.

NCT ID: NCT00348166 Withdrawn - Clinical trials for Refractive Error - Myopia

Does Undercorrection of Myopia Retard Myopia Progression Among Kindergarten Children?

Start date: December 2005
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find out if undercorrection of myopia slow down the progression of myopia in kindergarten children.

NCT ID: NCT00348127 Completed - Myopia Clinical Trials

A Singapore Pilot Study to Assess Neurovision in Treatment of Low Myopia

Start date: March 2003
Phase: Phase 1
Study type: Interventional

To assess how well and safe is Neurovision technology in improving the vision of people with low myopia in Singapore

NCT ID: NCT00348075 Completed - Myopia Clinical Trials

A Singapore Study to Assess How Neurovision Improve the Vision of Adults With Low to Moderate Myopia

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

To evaluate the efficacy of NeuroVision NVC vision correction technology to improve the vision of subjects with Low and Moderate Myopia in Asian eyes in Singapore

NCT ID: NCT00348049 Completed - Myopia Clinical Trials

Efficacy of LASIK Versus PRK in Asians With Mild and Moderate Myopia

Start date: November 2002
Phase: N/A
Study type: Interventional

Laser in situ keratomileusis (LASIK) and photorefractive keratectomy (PRK) are currently the 2 main refractive surgeries to correct myopia which are being performed worldwide, with more patients preferring LASIK to PRK because of better comfort and faster rehabilitation. However, in post-LASIK patients, there is a low risk of flap dislodgement. This risk increases with certain occupations which have a higher risk of trauma. Hence, there may be a role for PRK for people which such occupations, e.g. soldiers, parachutists, sportsman. There are several non-randomised studies which show that PRK is as efficacious, predictable and safe as LASIK for low to moderate myopes. But there have been only a few randomized controlled studies to compare the efficacy and safety of the 2 treatment modalities and all studies comparing LASIK and PRK suffer from a high dropout rate during the follow-up period. We compared the efficacy, predictability, stability and safety of LASIK versus PRK over a one year duration with almost 100% attendance during all follow-up visits.

NCT ID: NCT00347997 Withdrawn - Myopia Clinical Trials

A Study to Evaluate the Safety and Effectiveness of the 217z Laser With Zyoptix for Lasik

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

A Study to demonstrate the safety and efficacy of wavefront laser refractive surgery treatments for myopia and astigmatism.

NCT ID: NCT00347451 Completed - Glaucoma Clinical Trials

Optical Coherence Tomography Imaging of the Posterior Segment in High Myopia.

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

The prevalence of myopia in East Asia and Singapore in particular is amongst the highest in the world, with estimates ranging from 30-70% of the general population. Up to 30% of these are high myopes. High myopia is associated with degenerative changes in the fundus. It may also be associated with vision-threatening complications such as macular holes. The pathogenesis of macular holes in high myopes is not completely understood but is postulated to include a combination of anterior vitreous traction and posterior staphyloma formation and axial elongation. These forces lead to degenerative changes at the macula, including foveal detachment and retinoschisis that precede the formation of lamellar or full thickness macular holes. These changes are difficult to detect either clinically or by conventional imaging such as ultrasound, making efforts to correct them in the early stages with surgery difficult. High myopia is also associated with a two- to threefold increase in risk of developing glaucoma. However, the diagnosis of glaucoma in high myopes is difficult as many of the pathological changes in the myopic eye mimic those seen in glaucoma. The myopic optic disc in particular is notoriously difficult to differentiate from the glaucomatous disc. Currently, the diagnosis is highly subjective, relying on observations of the clinical appearance of the disc or on disc photos.Optical coherence tomography (OCT) is an evolving technology that relies on time delays of reflected or backscattered light and interferometry to yield cross-sectional images of the retina and optic disc. The Stratus OCT is the latest model and has been demonstrated to be able to yield images with a resolution comparable to that of histology. It is thus potentially useful in assessing degenerative changes occurring in the myopic fundus, in evaluating the early changes preceding macular hole formation, and in providing objective measures of various disc parameters to aid in diagnosing glaucoma in high myopes. This study aims to recruit 150 healthy, young, ophthalmologically normal males from the SAF and to examine them with OCT. High myopes (≤-8D) will be selected and compared with a control group of low myopes. The performance of the OCT will be evaluated against current diagnostic methods.