Trials / Completed
CompletedNCT00695435
Tobramycin Tear Concentrations
Evaluation of Tobramycin Tear Concentrations of TOBRADEX® Ophthalmic Suspension, Tobramycin 0.3% / Dexamethasone 0.05% Ophthalmic Suspension Versus TOBREX® Ophthalmic Solution in Normal Volunteers
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 21 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
To evaluate the Tobramycin tear concentration values of TOBRADEX® Ophthalmic Suspension, Tobramycin 0.3% / Dexamethasone 0.05% Ophthalmic Suspension versus TOBREX® Ophthalmic Solution in normal volunteers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | TOBRADEX Ophthalmic Suspension | TOBRADEX Ophthalmic Suspension 1 drop each eye at baseline |
| DRUG | Tobramycin 0.3% / Dexamethasone 0.05% Ophthalmic Suspension | Tobramycin 0.3% / Dexamethasone 0.05% Ophthalmic Suspension 1 drop each eye at baseline |
| DRUG | TOBREX Ophthalmic Solution | TOBREX Ophthalmic Solution 1 drop each eye at baseline |
Timeline
- Start date
- 2008-06-01
- Primary completion
- 2008-06-01
- First posted
- 2008-06-11
- Last updated
- 2010-03-02
- Results posted
- 2010-02-05
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00695435. Inclusion in this directory is not an endorsement.