Evaluation of the LipiFlow System With a New Activator

Status Completed

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

Meibomian Gland Dysfunction

Clinical Trial Details

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

View Details

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