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Safety and Efficacy of Dexamethasone (OZURDEX®) Intravitreal Implant in Korea

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Allergan

Status

Completed

Conditions

Retinal Vein Occlusion

Treatments

Drug: dexamethasone 700 ㎍ intravitreal implant

Study type

Observational

Funder types

Industry

Identifiers

NCT01976650
206207-029

Details and patient eligibility

About

This study is a Post-Market Surveillance study in Korea to evaluate the safety and efficacy of dexamethasone 700 ㎍ (OZURDEX®) intravitreal implant used to treat Branch Retinal Vein Occlusion, Central Retinal Vein Occlusion, or non-infectious uveitis affecting the posterior segment of the eye in clinical practice.

Enrollment

724 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with Branch Retinal Vein Occlusion, Central Retinal Vein Occlusion, or non-infectious uveitis affecting the posterior segment of the eye treated with (OZURDEX®) in clinical practice.

Exclusion criteria

  • Patients with eye infections
  • Patients with glaucoma.

Trial design

724 participants in 1 patient group

OZURDEX®
Description:
Patients who receive dexamethasone 700 ㎍ (OZURDEX®) intravitreal implant treatment for Branch Retinal Vein Occlusion, Central Retinal Vein Occlusion, or non-infectious uveitis affecting the posterior segment of the eye as per local standard of care in clinical practice.
Treatment:
Drug: dexamethasone 700 ㎍ intravitreal implant

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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