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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


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

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