Evaluation of an Investigational Lubricant Eye Drop on Lipid Layer Thickness

Alcon Research40 enrolled

Overview

The purpose of this study is to evaluate the effects of an investigational lubricant eye drop on tear film lipid layer thickness of dry eye patients.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Dry Eye

Interventions

ORB Ocular EmulsionOTHER

lubricant eye drop

SootheXP Emollient (Lubricant) Eye DropsOTHER

lubricant eye drop

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients (minimum age 18) meeting specific criteria for dry eye. Exclusion Criteria: * Use of topical ocular drops within 12 hours of the study visit; or use of topical ocular ointment within 36 hours of the study visit. In addition, cannot use any topical ocular drugs during study period. * History or evidence of ocular or systemic medical conditions and/or medications that would confound the evaluation.

Locations (1)

Alcon Call Center for Trial Locations

Fort Worth, Texas, United States

Outcomes

Primary Outcomes

Lipid layer thickness

Time frame: Baseline through 120 minutes post instillation

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.