Clinical Trials Directory

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

TypeNameDescription
DRUGBrimonidine 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.