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Clinical Trial Summary

The results of this trial will demonstrate that the iDesign System performs as intended and is acceptable in a clinical setting.


Clinical Trial Description

LASIK treatment across the range of myopia with or without astigmatism, hyperopia with or without astigmatism, and mixed astigmatism. ;


Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01220466
Study type Interventional
Source Abbott Medical Optics
Contact
Status Completed
Phase N/A
Start date October 2010
Completion date December 2011

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