CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 159 enrolled
Drug / intervention
SYSTANE® ULTRA Lubricant Eye Dropsdrug
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.

Search/NCT02446015
NCT02446015N/ACompleted
CompareCT.gov

Clinical Evaluation Following Use of SYSTANE® ULTRA in the Management of Dry Eye

Alcon Research·interventional·Posted May 15, 2015·Updated Jul 2, 2018

In Brief

A clinical study evaluating SYSTANE® ULTRA Lubricant Eye Drops for Dry Eye Syndrome. Completed, enrolled 159 participants.

Detailed Summary

The purpose of this study is to evaluate the clinical benefits of SYSTANE® ULTRA Lubricant Eye Drops using total ocular surface staining scores in subjects with dry eye administering it either as a scheduled regimen or as-needed after 28 days of treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDry Eye Syndrome
Countries--
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedMay 15, 2015
Enrollment StartJun 19, 2015
Primary CompletionJun 21, 2016
TodayJul 2, 2026
Enrollment to primary: 1.0 yearsPosted 11.1 years ago

Interventions

SYSTANE® ULTRA Lubricant Eye Dropsdrug