At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 51 enrolled
Drug / intervention
Cyclosporine 0.05% Ophthalmic Emulsiondrug
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.
Evaluation of Maintaining Visual Performance Of Subjects Who Engage in Electronic Visual Tasking While Using Restasis (EMPOWER)
In Brief
A Phase 4 clinical trial evaluating Cyclosporine 0.05% Ophthalmic Emulsion for Dry Eye Syndromes. Completed, enrolled 51 participants across 2 sites.
Detailed Summary
This study will evaluate the efficacy of Restasis® in participants with dry eye disease who engage in electronic visual tasking.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDry Eye Syndromes
CountriesUnited States
Collaborators--
Timeline
Phase 4CompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartJul 2015
First PostedSep 2015
Primary CompletionMar 2016
TodayJul 2026
First PostedSep 21, 2015
Enrollment StartJul 21, 2015
Primary CompletionMar 24, 2016
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 10.8 years ago
Interventions
Cyclosporine 0.05% Ophthalmic Emulsiondrug
Cyclosporine 0.05% Ophthalmic Emulsion (RESTASIS®) 1 drop instilled in each eye twice a day.