proxymetacaine and Staphylococcal Infections

proxymetacaine has been researched along with Staphylococcal Infections in 1 studies

proxymetacaine: RN given refers to parent cpd; structure

Staphylococcal Infections: Infections with bacteria of the genus STAPHYLOCOCCUS.

Research

Studies (1)

Authors

Clinical Trials (1)

Trial Overview

Trial Outcomes

Comfort With Intravitreal Injection Standard Procedure

Subjects were asked to complete a survey about their experience with intravitreal injections after the procedure was completed. The survey was scored on a 0 to 10 numeric rating scale (NRS) where 0 was a positive response and 10 was a negative response. The lower the score, the more comfortable the subject was with the procedure, the higher the score, the less comfortable the subject was with the procedure. (NCT02951351)
Timeframe: post-injection

Expectation Intravitreal Injection Will Have Negative Consequences on Subject Health

Subjects were asked to complete a survey about their experience with intravitreal injections after the procedure was completed. The survey was scored on a 0 to 10 numeric rating scale (NRS) where 0 was a positive response and 10 was a negative response. A lower score indicated subjects did not expect the injection would negatively affect their overall health. Higher scores indicated subjects expected the injection would negatively affect their overall health. (NCT02951351)
Timeframe: post-injection

Expectation the Injection Will Contribute to Curing/Improving Eye Condition

Patients were asked to rate their expectation on the extent to which the intravitreal injections would contribute to curing or improving their eye condition. The question was scored on a 0 to 10 numeric rating scale (NRS) where 0 was a negative response (not at all) and 10 was a positive response (to a large extent). A low score indicated the subject did not expect the injection would contribute to curing or improving the eye condition while a high score indicated the subject did expect the injection will help to cure or improve the eye condition. (NCT02951351)
Timeframe: post-injection

Impression of Pre-injection Preparations

Subjects were asked to complete a survey about their experience with intravitreal injections after the procedure was completed. The survey consisted of 6 questions and was scored on a 0 to 10 numeric rating scale (NRS) where 0 was a positive response and 10 was a negative response. The lower the score, the more positive impression of the preparation process, the higher the score, the less positive impression of the preparation process.. (NCT02951351)
Timeframe: post-injection

Number of Study Participants With Positive Conjunctival Culture

Conjunctival samples were collected after participants received either an additional drop of proparacaine or povidone iodine. Bacterial cultures were performed from conjunctival samples by the Mayo Clinic Microbiology laboratory. Bacterial species identification was performed on any and all bacteria that grew. (NCT02951351)
Timeframe: pre-injection

Overall Impression of Visit for Intravitreal Injection

Subjects were asked to complete a survey about their experience with intravitreal injections after the procedure was completed. The survey was scored on a 0 to 10 numeric rating scale (NRS) where 0 was a positive response and 10 was a negative response. The lower the score, the more positive impression of the visit, the higher the score, the less positive impression of the visit. (NCT02951351)
Timeframe: post-injection

Pain at the Time of Injection

Subjects were asked to complete a survey about their experience with intravitreal injections after the procedure was completed. The survey was scored on a 0 to 10 numeric rating scale (NRS) where 0 was a positive response and 10 was a negative response. The lower the score, the lesser the perceived pain, the higher the score, the higher the perceived pain. (NCT02951351)
Timeframe: post-injection

Residual Pain From Intravitreal Injection

Subjects were asked to complete a survey about their experience with intravitreal injections after the procedure was completed. The survey was scored on a 0 to 10 numeric rating scale (NRS) where 0 was a positive response and 10 was a negative response. The lower the score, the lesser the residual pain, the higher the score, the higher the residual pain. (NCT02951351)
Timeframe: post-injection

Trials

1 trial available for proxymetacaine and Staphylococcal Infections