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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
44
LipiFlow treatment with the Activators LFD-2100 will be performed on both eyes with MGD
Empire Eye and Laser Center
Bakersfield, California, United States
Wolstan & Goldberg Eye Associates
Torrance, California, United States
Texas Eye Research Center
Hurst, Texas, United States
Successful Completion of LipiFlow Treatment With Activator LFD-2100
Evaluation of the clinical use of the LipiFlow system with the Activator LFD-2100
Time frame: 1 day after completion of LipiFlow treatment
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