Expired Study
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Rochester, New York 14609


Purpose:

The objective of this study is to evaluate the safety of Besivance (besifloxacin ophthalmic suspension, 0.6%) compared to vehicle.


Criteria:

Inclusion Criteria: - Subjects must have a clinical diagnosis of acute bacterial conjunctivitis and exhibit purulent conjunctival discharge (crusty or sticky eyelids) and redness in at least one eye. - Subjects who are willing to discontinue contact lens wear for the duration of the study. - Subjects who are able and willing to comply with all treatment and follow- up/study procedures. Exclusion Criteria: - Subjects who have any uncontrolled systemic disease or debilitating disease. - Subjects with a known hypersensitivity or contraindications to Besivance, fluoroquinolones, or any of the ingredients in the study drugs. - Subjects who are expected to require disallowed concurrent systemic or ocular therapy(either eye)during or prior to study start. (ie, NSAIDs, corticosteroids, mast cell stabilizers, antihistamines, decongestants or antimicrobial therapy) - Subjects having ocular surgery (including laser surgery) in either eye within six weeks prior to entry into this study. - Subjects with suspected viral or allergic conjunctivitis or any other disease conditions that could interfere with the efficacy and safety evaluations of the study medication. - Subjects with suspected iritis. - Subjects with a history of recurrent corneal erosion syndrome, either idiopathic or secondary to previous corneal trauma or dry eye syndrome. - Subjects with any active ulcerative keratitis, specifically any epithelial loss greater than punctate keratitis. - Subjects who are immune compromised.


NCT ID:

NCT01175590


Primary Contact:

Study Director
Laura Trusso, MS
Bausch & Lomb, Inc.


Backup Contact:

N/A


Location Contact:

Rochester, New York 14609
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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