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NCT06710951: anti-VEGF

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

Completed NA Last updated 29 November 2024
What this trial tests

NA trial testing Change of normal concentration of povidone-iodine 5% to 1% in Dry Eye in 88 participants. Completed in 30 June 2022.

Timeline
15 November 2021
Primary endpoint
30 June 2022
30 June 2022

Quick facts

Lead sponsorJosé Gerardo García Aguirre
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment88
Start date15 November 2021
Primary completion30 June 2022
Estimated completion30 June 2022
Sites1 location across Mexico

Drugs / interventions tested

Conditions studied

Sponsor

José Gerardo García Aguirre

Who can join

45 and older, any sex, with Dry Eye. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Dry Eye

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06710951.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing