At a glance
ClinicalIndex Comparison RecordN/ACompleted· 207 enrolled
Drug / intervention
Polyethylene Glycol, 0.4%, Propylene Glycol, 0.3% eye dropsother
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.
Clinical Evaluation of Systane® Gel Drops on Corneal Staining in Indian Subjects With Dry Eye
In Brief
A clinical study evaluating Polyethylene Glycol, 0.4%, Propylene Glycol, 0.3% eye drops for Dry Eye. Completed, enrolled 207 participants across 1 site.
Detailed Summary
The purpose of this study is to evaluate the efficacy and safety of Systane® Gel Drops in dry eye subjects following 90 days of QID (4 times/day) dosing.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDry Eye
CountriesIndia
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedMar 2015
Enrollment StartMay 2015
Primary CompletionJun 2016
TodayJul 2026
First PostedMar 5, 2015
Enrollment StartMay 14, 2015
Primary CompletionJun 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1.0 yearsPosted 11.3 years ago
Interventions
Polyethylene Glycol, 0.4%, Propylene Glycol, 0.3% eye dropsother