Clinical Trials Directory

Trials / Completed

CompletedNCT05069350

Bupivacaine vs Oxybuprocaine Topical Anesthesia in IVI

A Double Blinded Randomized Controlled Study of Topical Anaesthetics Oxybuprocaine Versus Bupivacaine 0.5% in Intravitreal Injections

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Research Institute of Ophthalmology, Egypt · Academic / Other
Sex
All
Age
30 Years – 70 Years
Healthy volunteers
Accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGbupivacaine 0.5% and oxubuprocaineusing each drug as surface anesthesia before intravitreal injections

Timeline

Start date
2021-09-01
Primary completion
2022-08-01
Completion
2022-08-01
First posted
2021-10-06
Last updated
2022-09-13

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05069350. Inclusion in this directory is not an endorsement.