At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 50 enrolled
Drug / intervention
Olopatadine 0.1% +3 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.
Efficacy Investigation Study of Olopatadine Hydrochloride Ophthalmic Solution Using OHIO Chamber in Patients With Seasonal Allergic Rhinitis (SAR)
In Brief
A Phase 4 clinical trial evaluating Olopatadine 0.1%, Tranilast 0.5%, and 2 other interventions for Allergic Conjunctivitis. Completed, enrolled 50 participants.
Detailed Summary
To evaluate the efficacy of olopatadine 0.1% using the OHIO Chamber in patients with seasonal allergic conjunctivitis.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAllergic Conjunctivitis
Countries--
Collaborators--
Timeline
Phase 4CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartJul 2008
Primary CompletionJul 2008
First PostedJan 2009
TodayJul 2026
First PostedJan 8, 2009
Enrollment StartJul 1, 2008
Primary CompletionJul 1, 2008
TodayJul 2, 2026
Enrollment to primary: 0 daysPosted 17.5 years ago
Interventions
Olopatadine 0.1%drug
one drop in one eye
Tranilast 0.5%drug
one drop in one eye
Placebo (Olopatadine)drug
one drop in contralateral eye
Placebo (Tranilast)drug
one drop in contralateral eye