At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 40 enrolled
Drug / intervention
dexamethasone intraocular suspension, 9% +1 moredrug
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 Intraoperative Use of Dexycu on the Signs and Symptoms of Dry Eye
In Brief
A Phase 4 clinical trial evaluating dexamethasone intraocular suspension, 9% and Prednisolone Acetate 1% Oph Susp for Dry Eye Syndromes. Completed, enrolled 40 participants across 1 site.
Detailed Summary
To compare the signs and symptoms of dry eye after cataract surgery between subjects randomized to receive intraoperative dexamethasone in addition to the use of a standard topical post-op treatment regimen.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDry Eye Syndromes
CountriesUnited States
Collaborators--
Timeline
Phase 4CompletedFinished
2020202120222023202420252026
Enrollment StartAug 2019
Primary CompletionDec 2019
First PostedDec 2019
TodayJul 2026
First PostedDec 4, 2019
Enrollment StartAug 10, 2019
Primary CompletionDec 1, 2019
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 6.6 years ago
Interventions
dexamethasone intraocular suspension, 9%drug
single dose intracameral corticosteroid
Prednisolone Acetate 1% Oph Suspdrug
topical ophthalmic steroid drop