Prospective, Randomized, Masked, Controlled Trial To Evaluate The Safety And Effectiveness Of The TearCare® System In The Treatment Of The Signs And Symptoms Of Dry Eye Disease (SAHARA)

NAActive, not recruitingINTERVENTIONAL
Enrollment

350

Participants

Timeline

Start Date

April 23, 2021

Primary Completion Date

March 22, 2024

Study Completion Date

May 22, 2024

Conditions
Dry EyeMeibomian Gland Dysfunction
Interventions
DEVICE

TearCare System

TearCare procedures in this study will include an in-office eyelid debridement, 15 minute bilateral thermal session with the TearCare System, immediately followed by manual expression of the meibomian glands using the Clearance Assistant Plus device. Subjects randomized to TearCare will receive one in-office TearCare procedure within 7 days of the Baseline visit and at 5 Months. Beginning at 9 Months, subjects will receive an additional TearCare procedure when TBUT drops lower than Baseline or within 2 seconds of baseline AND/OR if OSDI worsens by at least 1 category.

DRUG

Restasis

Restasis group will be required to self-administer 1 drop twice a day from baseline through the Month 6 visit. At Month 6, subjects will be crossed over to the TearCare group and will receive one (1) TearCare procedure.

Trial Locations (14)

15213

University of Pittsburg-Ophthalmology Dept, Pittsburgh

19004

Vantage Eye Care, Bala-Cynwyd

28150

Vita Eye Clinic, Shelby

33143

Loh Ophthalmology Associates, Miami

40517

Kentucky Eye Institute, Lexington

41017

Cincinnati Eye Institute, Edgewood

57108

Vance Thompson Vision, Sioux Falls

60046

Jackson Eye, Lake Villa

78229

Parkhurst NuVision, San Antonio

80907

Vision Institute, Colorado Springs

85254

Doctor My Eyes, Scottsdale

92037

Scripps Health, La Jolla

92653

Harvard Eye Associates, Laguna Hills

92663

Eye Research Foundation, Newport Beach

All Listed Sponsors
lead

Sight Sciences, Inc.

INDUSTRY