Trials / Completed
CompletedNCT01493427
Efficacy of Changing to TRAVATAN® From Prior Therapy
Multi-Center Study Assessing the Efficacy and Tolerability of TRAVATAN® Solution Without BAK, Containing Polyquad® Preservative (0.004% Travoprost) in Patients Previously on Latanoprost 0.005% or Bimatoprost 0.01% Ophthalmic Solution Monotherapy
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 202 (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 benzalkonium chloride (BAK) in patients previously on latanoprost 0.005% or bimatoprost 0.01% ophthalmic solution monotherapy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Travoprost 0.004% | Travoprost 0.004% without benzalkonium chloride (BAK), containing Polyquad (PQ) preservative |
Timeline
- Start date
- 2011-12-01
- Primary completion
- 2013-02-01
- Completion
- 2013-02-01
- First posted
- 2011-12-16
- Last updated
- 2014-05-19
- Results posted
- 2014-05-09
Source: ClinicalTrials.gov record NCT01493427. Inclusion in this directory is not an endorsement.