Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery

Bausch + Lomb

Status and phase: Completed; Phase 3

Conditions: Cataract

Treatments: Drug: bromfenac ophthalmic solution; Drug: placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT00703781

CL-S&E-0415081-P-ER

Details and patient eligibility

About

Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery

Enrollment: 126 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Scheduled for cataract surgery

Exclusion criteria

• Known hypersensitivity to bromfenac and salicylates

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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126 participants in 2 patient groups, including a placebo group

Bromfenac

Experimental group

Description:

Bromfenac Ophthalmic Solution 0.09%, Dosed 1 Drop Daily

Treatment:

Drug: bromfenac ophthalmic solution

Placebo

Placebo Comparator group

Description:

Placebo, Dosed 1 Drop Daily

Treatment:

Drug: placebo