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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Change 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.