Clinical Trials Directory

Trials / Completed

CompletedNCT06710951

Effect of Povidone-iodine 5% Vs 1% on the Ocular Surface in Intravitreal Injections of Anti-VEGF

Effect of Povidone-iodine 5% Vs 1% on the Ocular Surface As Antiseptic for Anti Vascular Endothelial Growth Factor Intravitreal Injections

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
88 (actual)
Sponsor
José Gerardo García Aguirre · Academic / Other
Sex
All
Age
45 Years
Healthy volunteers
Not accepted

Summary

Objective and subjective comparison between the use of povidone-iodine 1% vs 5% as antiseptic in patients that need anti-VEGF intravitreal injection

Detailed description

Randomized, prospective clinical trial. One group was intervened with povidone-iodine at 5% and the other at 1% as antiseptic for anti-VEGF intravitreal injection. Each patient was evaluated before and after the injection of anti-VEGF for tear break up time, bulbar redness and ocular surface satining with fluorescein. Pain perception was also evaluated 15 minutes after the injection and 48 hours after.

Conditions

Interventions

TypeNameDescription
PROCEDUREChange of normal concentration of povidone-iodine 5% to 1%Normal concentration of povidone-iodine during anti-VEGF intravitreal injection was 5%. That concentration was utilized in the control group, and 1% in the experimental group.

Timeline

Start date
2021-11-15
Primary completion
2022-06-30
Completion
2022-06-30
First posted
2024-11-29
Last updated
2024-11-29

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT06710951. Inclusion in this directory is not an endorsement.