CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 371 enrolled
Drug / intervention
Travoprost 0.004% (POLYQUAD-preserved) Eye Drops, Solution +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.

Search/NCT00848536
NCT00848536Phase 3Completed

A Multi-Center, Double-Masked Study of the Safety and Efficacy of Travoprost APS Compared to TRAVATAN® in Patients With Open-Angle Glaucoma or Ocular Hypertension

Alcon Research·interventional·Posted Feb 20, 2009·Updated Apr 6, 2012

In Brief

A Phase 3 clinical trial evaluating Travoprost 0.004% (POLYQUAD-preserved) Eye Drops, Solution and Travoprost 0.004% (BAK-preserved) Eye Drops, Solution for Open Angle Glaucoma and Ocular Hypertension. Completed, enrolled 371 participants.

Detailed Summary

A Multi-Center Double-masked Study of the Safety and Efficacy of Travoprost APS Compared to TRAVATAN in Patients with Open-angle Glaucoma or Ocular Hypertension

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

Phase 3CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedFeb 20, 2009
Enrollment StartMar 1, 2009
Primary CompletionJan 1, 2010
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 17.4 years ago

Interventions

Travoprost 0.004% (POLYQUAD-preserved) Eye Drops, Solutiondrug

One drop once daily in the evening for 3 months

Travoprost 0.004% (BAK-preserved) Eye Drops, Solutiondrug

One drop once daily in the evening for 3 months