Effect of Bromfenac on Pain Related to Pterygium Surgery

Status Completed

Clinical Trial Summary

To evaluate the efficacy and ocular safety of bromfenac ophthalmic solution (bromfenac) 0.1% dosed twice daily for the treatment of ocular inflammation and pain after pterygium excision with amniotic membrane transplantation(AMT).

Clinical Trial Description

Patients scheduled to undergo pterygium excision with AMT were randomized to receive added topical bromfenac or artificial lacrima at 3 days before and 7 days after the surgery. Pain intensity was evaluated with the visual analog scale(VAS) and present pain index(PPI) with the short form of the McGill Pain Questionnaire. psychological state used Self-rating of Depression Scale(SDS) and Self-rating of Anxiety Scale (SAS) to assess. Ocular inflammation was assessed with an automated bulbar redness grading technique. The irritative symptoms evaluation was carried out by an independent investigator at each visit with questionnaires of ocular symptom scores(OSS). Corneal epithelial healing rate was calculated after following up. All patients had follow-ups at the day 1, day 3, day7 and day 10. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04022811
Study type	Interventional
Source	Zhongshan Ophthalmic Center, Sun Yat-sen University
Contact
Status	Completed
Phase	Phase 4
Start date	October 2016
Completion date	October 2017

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