Status:

COMPLETED

Povidone Iodine vs AVEnova: A Pre-injection Disinfection Study (PAVE Study)

Lead Sponsor:

California Retina Consultants

Conditions:

Age-related Macular Degeneration

Diabetic Retinopathy

Eligibility:

All Genders

18+ years

Phase:

PHASE4

Brief Summary

To compare the efficacy and comfort of two FDA approved pre-injection antiseptics when used for intravitreal injections.

Detailed Description

Intravitreal injection of medicine has become the most common ocular procedure billed to Medicare. One of the main problems with this procedure is the postoperative discomfort due to the need to disin...

Eligibility Criteria

Inclusion

  • Subjects must be receiving same day bilateral injections of an anti-VEGF agent for any ophthalmic condition.
  • Subject must be fluent in English.

Exclusion

  • Under 18 years old.
  • Subjects with an allergy or adverse reaction to Povidone Iodine or Avenova.

Key Trial Info

Start Date :

July 16 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 14 2019

Estimated Enrollment :

50 Patients enrolled

Trial Details

Trial ID

NCT04018482

Start Date

July 16 2019

End Date

August 14 2019

Last Update

March 10 2020

Active Locations (1)

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California Retina Consultants

Santa Barbara, California, United States, 93103