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Bromfenac Sodium Hydrate Eye Drops in Familial Exudative Vitreoretinopathy

Recruiting
1 - 7 years of age
Both
Phase 2
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Overview

This study aims to investigate the efficacy and safety of bromfenac sodium hydrate eye drops in patients with familial exudative vitreoretinopathy receiving diode laser photocoagulation.

Description

This study aims to evaluate the presence of macular edema as the primary measure and the presence of conjunctival injection as the secondary measure for the investigation of the efficacy of bromfenac sodium hydrate eye drops in patients with familial exudative vitreoretinopathy receiving diode laser photocoagulation.

Eligibility

Inclusion Criteria:

  • Newly diagnosed patients with familial exudative vitreoretinopathy
  • Needing diode laser photocoagulation
  • Consent to the study

Exclusion Criteria:

  • History of corneal diseases
  • History of hypersensitivity to bromfenac sodium
  • History of hypersensitivity to non-steroidal anti-inflammatory drugs
  • Progressive ocular infection
  • Liver diseases
  • Hypersensitivity to sulfur dioxide
  • Receiving anti-coagulation drugs
  • History of coagulopathies

Study details

Familial Exudative Vitreoretinopathies

NCT05107921

Seoul National University Hospital

25 January 2024

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