A Pilot Study of the TearCare System in Adults With Dry Eye Disease

NCT03006978 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2025-10-15

Study results available
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Summary

This is a small, pilot study intended to determine the feasibility of this product.

Conditions

  • Dry Eye

Interventions

DEVICE

TearCare

DEVICE

Warm Compress

Sponsors & Collaborators

  • Sight Sciences, Inc.

    lead INDUSTRY

Principal Investigators

  • David Badawi, MD · Sight Sciences

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2017-02-28
Completion
2018-03-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03006978 on ClinicalTrials.gov