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Clinical Trial Summary

Study to evaluate the safety and efficacy of HI-BRITE large diameter rigid gas permeable contact lens (hexafocon b) test when worn on a daily wear basis in the correction of myopia/hyperopia/astigmatism/presbyopia/ and irregular cornea.


Clinical Trial Description

Subjects who meet all eligible requirements for entry into the study will be instructed to insert the Hi-Brite Large Diameter Rigid Gas Permeable contact lens in daily wear basis for clinical evaluation purposes.

Treatment period: 6 months ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02812316
Study type Interventional
Source Taipei Medical University Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date August 2014
Completion date October 2017

See also
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