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Efficacy and Safety of PRO-155 Versus Nevanac in Post Phacoemulsification

Cataract Clinical Trial

Official title:
Phase 2 Randomized, Double-blind Clinical Trial to Evaluate Efficacy and Safety of the Ophthalmic Solution PRO-155 Versus Nevanac 0.1% Ophthalmic Solution in Post Phacoemulsification Patients

Clinical Trial Summary

The purpose of this study is to evaluate efficacy and safety of the ophthalmic solution PRO-155 in patients post phacoemulsification.

Clinical Trial Description

Postsurgical inflammation is an inevitable condition after cataract surgery. The use of non-steroidal anti-inflammatory drugs is a safe option for treating ocular inflammation.

This is a phase II randomized double-blind clinical trial. The aim is to compare and to evaluate efficacy and safety of two ophthalmic solutions in patients post phacoemulsification. Patients will be randomized to receive either PRO-155 or Nevanac for 60 days. ;

Study Design

Related Conditions & MeSH terms

  • Cataract
  • Phacoemulsification Cataract Surgery
Clinical Trial Details
NCT number NCT01657266
Study type Interventional
Source Laboratorios Sophia S.A de C.V.
Contact
Status Completed
Phase Phase 2
Start date December 2013
Completion date April 2015
View Details
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