An interventional study of Brimonidine Purite in Cataract, sponsored by Indiana University. Completed at 4 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2007-10-17.
Sponsored by Indiana University · Not applicable, Interventional, and Treatment
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)
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.
1,726 studies on the registry are indexed under Cataract; 230 are open to participants now.
This study's enrollment of 22 is below the median of 80 across 1,171 interventional studies indexed under Cataract.
Browse Cataract studies →Indiana University is the lead sponsor of 982 studies on the registry; 199 are open to participants now.
Of its 148 completed or terminated interventional studies of FDA-regulated products, 117 (79%) have results posted.
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All subjects must:
Exclusion Criteria:
No subject may:
Bioanalysis of brimonidine concentrations.
This study is completed, as verified in Oct 2007. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: Brimonidine