Trials / Completed
CompletedNCT01510145
Efficacy of Changing to TRAVATAN® From Prior Therapy
Multi-Center Study Comparing Efficacy and Tolerability of TRAVATAN® BAK-free (0.004% Travoprost) in Patients Previously on Latanoprost Ophthalmic Solution 0.005% Monotherapy
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 191 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study was to assess the efficacy and tolerability of TRAVATAN® solution without BAK (benzalkonium chloride) after changing from prior latanoprost 0.005% ophthalmic solution monotherapy in subjects with open-angle glaucoma or ocular hypertension due to tolerability issues.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Travoprost 0.004% BAK-free | Containing Polyquad (PQ) preservative |
Timeline
- Start date
- 2012-02-01
- Primary completion
- 2013-05-01
- Completion
- 2013-05-01
- First posted
- 2012-01-13
- Last updated
- 2014-06-13
- Results posted
- 2014-06-13
Source: ClinicalTrials.gov record NCT01510145. Inclusion in this directory is not an endorsement.