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A Safety and Efficacy Study to Assess OZURDEX® in Patients With Macular Oedema Secondary to Retinal Vein Occlusion (RVO)

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Allergan

Status

Completed

Conditions

Macular Edema
Retinal Vein Occlusion

Treatments

Drug: dexamethasone 700 ug intravitreal implant

Study type

Observational

Funder types

Industry

Identifiers

NCT01571557
MAF/AGN/OPH/RET/011

Details and patient eligibility

About

This study will evaluate the relationship between time since onset of macular oedema symptoms and the achievement of vision gain in patients prescribed OZURDEX®. All care and diagnostic procedures provided are at the discretion of the participating physicians according to their clinical judgment and local standard of medical care.

Enrollment

573 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of macular edema following retinal vein occlusion
  • Prescribed OZURDEX®

Exclusion criteria

  • Previous treatment with OZURDEX®

Trial design

573 participants in 1 patient group

OZURDEX®
Description:
OZURDEX® (dexamethasone 700 ug intravitreal implant) administered according to standard of care.
Treatment:
Drug: dexamethasone 700 ug intravitreal implant

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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