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Topical Bromfenac for Intraoperative Miosis and Pain Reduction

Cataract Clinical Trial

Official title:
Topical 0,09% Bromfenac for Intraoperative Miosis and Pain Reduction in Femtosecond Laser-assisted Cataract Surgery

Clinical Trial 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.

Clinical Trial Description

This prospective cross-sectional randomized clinical study included 60 patients with senile cataract in the absence of significant ocular comorbidity. The patients received 0.09% bromfenac ophthalmic solution or control placebo twice a day for 3 days before surgery. Pupil diameter was measured at the initiation and finalization of femtosecond laser-assisted cataract surgery and pain quantification was assessed by analogous pain scale at one day follow-up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03831984
Study type Interventional
Source Hospital de La Luz
Contact
Status Enrolling by invitation
Phase Phase 4
Start date March 1, 2018
Completion date March 30, 2019
View Details
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