Status:

COMPLETED

Treatment of CNV With Aflibercept Combined With Pranoprofen Eye Drops or Nutraceutical Support With Omega-3

Lead Sponsor:

Università degli Studi di Brescia

Conditions:

Macular Edema

Eligibility:

All Genders

40+ years

Phase:

PHASE4

Brief Summary

To determine whether a combination of intravitreal aflibercept and pranoprofen eyedrops or nutraceutical support provides additional benefit over IVA monotherapy for the treatment of choroidal neovasc...

Eligibility Criteria

Inclusion

  • provision of written informed consent and compliance with study assessments for the full duration of the study
  • age \> 40 years
  • presence of treatment-naïve neovascular AMD.

Exclusion

  • any previous intravitreal treatment
  • previous laser treatment in the study eye
  • myopia \> 7 diopters in the study eye
  • concurrent eye disease in the study eye that could compromise visual acuity (e.g., diabetic retinopathy and advanced glaucoma)
  • concurrent corneal epithelial disruption or any condition that would affect the ability of the cornea to heal
  • known sensitivity to any component of the formulations being investigated.

Key Trial Info

Start Date :

January 1 2016

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2017

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT03355638

Start Date

January 1 2016

End Date

July 1 2017

Last Update

November 28 2017

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