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Clinical Trial Summary

comparing two local anaesthetic agents, Bupivacaine 0.5% versus Oxybuprocaine used topically to provide surface anaesthesia before IVI procedures.


Clinical Trial Description

In preparation zone, we will cannulate the patients, connect them to the pulse oximetry and we will start providing appropriate surface anaesthesia for an adequate period of time before the patient administration of the injection, by applying the anaesthetic agents, 3 times with 5 minutes interval, for 15 minutes and then waitng the injection All patients are informed that they are going to receive topical anaesthetic agent before the IVI. pain is monitored during the injection by using the 11 points verbal numerical pain scaling as zero is for no pain and 10 is for severe unbearable pain. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05069350
Study type Interventional
Source Research Institute of Ophthalmology, Egypt
Contact
Status Completed
Phase Early Phase 1
Start date September 1, 2021
Completion date August 1, 2022

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