Overview

Topical Bromfenac for Intraoperative Miosis and Pain Reduction

Status:
Unknown status
Trial end date:
2019-03-30
Target enrollment:
0
Participant gender:
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 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Hospital de La Luz
Treatments:
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