At a glance
ClinicalIndex Comparison RecordN/ACompleted· 51 enrolled
Drug / intervention
Propylene glycol 0.6% ocular emulsion +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
The Effect of SYSTANE® BALANCE on Non-Invasive Tear Film Break Up Time (NITFBUT) in Dry Eye Subjects With Lipid Deficiency Following 30 Days of Use
In Brief
A clinical study evaluating Propylene glycol 0.6% ocular emulsion and Sodium chloride 0.9% saline solution for Dry Eye. Completed, enrolled 51 participants across 1 site.
Detailed Summary
The purpose of this study was to evaluate the ability of SYSTANE® BALANCE dosed 4 times a day for 30 days to increase non-invasive tear film break up time over baseline, compared to a saline control, in dry eye subjects with lipid deficiency.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDry Eye
CountriesArgentina
Collaborators--
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartSep 2012
Primary CompletionOct 2012
First PostedOct 2012
TodayJul 2026
First PostedOct 31, 2012
Enrollment StartSep 1, 2012
Primary CompletionOct 1, 2012
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 13.7 years ago
Interventions
Propylene glycol 0.6% ocular emulsionother
Sodium chloride 0.9% saline solutionother