At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 32 enrolled
Drug / intervention
Travoprost Ophthalmic Solution 0.004%drug
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.
Investigation of the Effect of Travoprost Ophthalmic Solution of Lowering Intraocular Pressure in Patients With Normal Tension Glaucoma
In Brief
A Phase 4 clinical trial evaluating Travoprost Ophthalmic Solution 0.004% for Normal Tension Glaucoma and Ocular Hypertension. Completed, enrolled 32 participants across 1 site.
Detailed Summary
The purpose of this study is to investigate IOP reduction efficacy of travoprost 0.004% ophthalmic solution (TRAVATAN Z®) in subjects with normal tension glaucoma.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsNormal Tension Glaucoma, Ocular Hypertension
CountriesJapan
Collaborators--
Timeline
Phase 4CompletedFinished
2014201520162017201820192020202120222023202420252026
Enrollment StartSep 2013
First PostedNov 2013
Primary CompletionJun 2014
TodayJul 2026
First PostedNov 26, 2013
Enrollment StartSep 1, 2013
Primary CompletionJun 1, 2014
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 12.6 years ago
Interventions
Travoprost Ophthalmic Solution 0.004%drug
benzalkonium chloride (BAC) free