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COMPLETED
NCT07639034
PHASE4

Effectiveness of Systane PRO for Mild to Moderate Dry Eye Disease

Sponsor: Gordon Schanzlin New Vision

View on ClinicalTrials.gov

Summary

The primary objective of this study is to show that consistent use of Systane PRO over a 30 period will significantly improve the signs and symptoms of Dry Eye Disease and decrease patients' ocular surface disease index score for patients diagnosed with mild-moderate (DED).

Official title: The Effectiveness of Systane PRO in Providing Relief From Multiple Symptoms of Dry Eye Disease and Its Impact on Daily Functioning and Overall Comfort in Patients With Mild to Moderate Dry Eye Disease

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

33

Start Date

2025-11-01

Completion Date

2026-02-01

Last Updated

2026-06-17

Healthy Volunteers

No

Interventions

DRUG

Systane Pro Topical Ophthalmic

To show that consistent use of Systane PRO will significantly improve the signs and symptoms of Dry Eye Disease in patients with mild-moderate DED.

Locations (1)

Gordon Schanzlin New Vision Institute

La Jolla, California, United States