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Clinical Trial Summary

The purpose of this clinical study is to evaluate the on-eye performance of an investigational soft contact lens compared to a commercially available soft contact lens following 1 week of extended wear.


Clinical Trial Description

Subjects will be randomized to wear the investigational contact lens in 1 eye and the commercially available contact lens in the other eye. Subjects will be expected to attend 3 scheduled study visits: Day 1 Baseline/Dispense; Day 2 Follow-up; and Week 1 Follow-up/Exit. The expected duration of exposure to each of the study lenses for all randomized, completed subjects was approximately 7 days / 6 nights of wear. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03614130
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date August 23, 2018
Completion date September 11, 2018

See also
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