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Clinical Trial Summary

This study aimed to compare the efficacy between 2% lidocaine gel vs 0.5% tetracaine eye drop as topical anesthesia in phacoemulsification


Clinical Trial Description

Approval from Ethical Committee of Faculty of Medicine Universitas Indonesia was acquired prior conducting the study. Subjects were given informed consent before enrolling the study and randomized into two groups (Lidocaine gel and tetracaine eye drop group). Lidocaine group received 2% lidocaine gel in 1 ml syringe, applied to the eye. Tetracaine group received 0.5% tetracaine eye drop. Topical anesthesia was given 5 minutes before phacoemulsification. Five minutes after phacoemulsification finished, visual analog score (VAS) and subjects and surgeon's satisfaction were assessed. Every additional topical anesthesia needed was recorded. ;


Study Design


Related Conditions & MeSH terms

  • Adult Patients Undergoing Phacoemulsification With Topical Anesthesia

NCT number NCT03143452
Study type Interventional
Source Indonesia University
Contact
Status Completed
Phase N/A
Start date December 1, 2016
Completion date January 31, 2018