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Clinical Trial Summary

Minimum 50 eyes and up to 100 eyes will be treated in this prospective, open-label clinical study. The investigator or designee will perform LipiFlow treatment with the Activators LFD-2100 on both eyes of a subject. The data from the treatment reports generated by the LipiFlow console and from the questionnaire will be used to assess the clinical utilization of the Activator LFD-2100. This study will be conducted in up to four sites in the USA.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04500821
Study type Interventional
Source Johnson & Johnson Surgical Vision, Inc.
Contact
Status Completed
Phase N/A
Start date October 2, 2020
Completion date October 30, 2020

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