Overview
Topical Bromfenac for Intraoperative Miosis and Pain Reduction
Status:
Unknown status
Unknown status
Trial end date:
2019-03-30
2019-03-30
Target enrollment:
0
0
Participant gender:
All
All
Summary
To evaluate the effect of bromfenac ophthalmic solution 0.09% for reduction of intraoperative miosis and pain in patient who have undergone femtosecond laser-assisted cataract surgery.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Hospital de La LuzTreatments:
Bromfenac
Hyaluronic Acid
Criteria
Inclusion Criteria:- Male and female
- Subjects 18 years or older
- Patients scheduled for unilateral femtosecond laser-assisted cataract surgery cataract
surgery with posterior chamber (PC) IOL implantation.
Exclusion Criteria:
- Presence of corneal abnormalities
- History of intraocular surgery
- History of ocular or systematic diseases (glaucoma, diabetes, uveitis
- Regular, systemic use of steroid or NSAIDs during the previous 3 months