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Clinical Trial Summary

The specific aims of this study are to compare patient experience with and without a proparacaine drop after povidone iodine.


Clinical Trial Description

To ensure the extra drop does not interfere with antisepsis, conjunctival cultures will be obtained from patients undergoing intravitreal injection before and after the application of the extra eye drop. Patients will be randomized to undergo additional topical analgesia during intravitreal injection vs. the standard amount of topical analgesia. Cultures of the eyelid/conjunctiva will be taken to ensure that the additional topical analgesia does not interfere with antisepsis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02951351
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase N/A
Start date October 12, 2016
Completion date February 2018

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