A Usability Study of iTEAR100 For Combined EyeLid Microblepharoexfoliation and Neurostimulation

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The purpose of this study is to evaluate the usability of the iTEAR100 generation 2 device in combination with its newly developed iLIDS100 disposable cover.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Must use iTEAR and NuLids at time of enrollment

Locations
United States
Washington
Olympic Ophthalmics
RECRUITING
Issaquah
Contact Information
Primary
Michael Gertner, MD
mgertner@oo-med.com
650-283-9388
Time Frame
Start Date: 2024-01-19
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 200
Treatments
Experimental: Therapeutic iLIDS arm
Subjects apply iTEAR100 device with iLIDS100 accessory
Related Therapeutic Areas
Sponsors
Leads: Olympic Ophthalmics, Inc.

This content was sourced from clinicaltrials.gov

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