Overview
Evaluation of Comfort With Xibrom (Bromfenac Ophthalmic Solution)0.09% and Nevanac (Nepafenac Ophthalmic Suspension) 0.1% Following Selective Laser Trabeculoplasty (SLT)
Status:
Completed
Completed
Trial end date:
2009-06-01
2009-06-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The objective of this study is to evaluate and compare the comfort of bromfenac or nepafenac following SLT.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Bp Consulting, IncTreatments:
Anti-Inflammatory Agents, Non-Steroidal
Bromfenac
Nepafenac
Ophthalmic Solutions
Criteria
Inclusion Criteria:- > 18 years old, either gender or any race.
- Diagnosis of open-angle glaucoma or ocular hypertension requiring laser
trabeculoplasty.
- Completion of written and informed consent/authorization prior to any study related
procedures.
- Able to follow study protocol and likely to complete study schedule.
Exclusion Criteria:
- Known sensitivity to NSAIDs.
- History of neovascular or ocular inflammatory disease.
- Current use of topical or systemic anti-inflammatory medications.
- Females of childbearing potential.