Trials / Completed
CompletedNCT00352807
Absorption of Brimonidine Ophthalmic Solution in the Aqueous Humor of Cataract Patients
Absorption of Brimonidine Ophthalmic Solution in the Aqueous Humor of Cataract Patients.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 22 (planned)
- Sponsor
- Indiana University School of Medicine · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to obtain and assay human aqueous samples following pre-operative dosing with 0.1% Brimonidine Purite™ (pH 7.8) or with 0.15% Brimonidine Purite® (pH 7.2) from patients undergoing routine cataract surgery in order to evaluate the aqueous concentration of the two formulations.Study hypothesis: The aqueous humor concentration 45 minutes following dosing of 0.1% Brimonidine Purite™ (pH 7.8) is comparable with 0.15% Brimonidine Purite® (pH 7.2)
Detailed description
The purpose of this study is to obtain and assay human aqueous samples following pre-operative dosing with 0.1% Brimonidine Purite™ (pH 7.8) or with 0.15% Brimonidine Purite® (pH 7.2) from patients undergoing routine cataract surgery in order to evaluate the aqueous concentration of the two formulations.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Brimonidine Purite |
Timeline
- Start date
- 2005-02-01
- Completion
- 2005-12-01
- First posted
- 2006-07-17
- Last updated
- 2007-10-17
Locations
4 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00352807. Inclusion in this directory is not an endorsement.