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Clinical Trial Summary

Evaluation of saline solutions used with scleral rigid gas permeable contact lens wearers experiencing debris in the post lens tear reservoir


Clinical Trial Description

One-month, approximately 36 subjects enrolled (~12/site), randomized, double-masked crossover trial. Existing scleral rigid gas permeable (RGP) contact lens wearing subjects are randomly assigned (block) to different arms of the trial and receive different saline solutions for use sequentially for 2-week periods. The subjects will continue to wear their existing scleral GP lenses if lens fit is acceptable following an initial evaluation. Subjects will agree to complete a survey administered daily (via email) that will address contact lens wear time and subjective symptoms. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03525704
Study type Interventional
Source Contamac Ltd
Contact
Status Completed
Phase N/A
Start date April 9, 2018
Completion date December 15, 2018

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