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Evaluation of SYSTANE® BALANCE in Dry Eye Subjects With Lipid Deficiency

NCT01688726 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 91

Last updated 2018-06-29

Study results available
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Summary

The purpose of this study is to evaluate the repeated use of SYSTANE® BALANCE on stabilizing the tear film of dry eye patients with an unstable tear film.

Conditions

  • Dry Eye Syndrome
  • Lipid Deficiency

Interventions

OTHER

SYSTANE® BALANCE eyedrops

OTHER

Minims® Saline 0.9% eyedrops

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Michel Guillon, PhD, FCOptom, FAAO, CCTI · OTG Research & Consultancy

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-12-31
Primary Completion
2013-11-30
Completion
2013-11-30

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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 NCT01688726 on ClinicalTrials.gov