drugset / Trial / NCT02093689

Intraoperative Floppy Iris Syndrome Undergoing Intraocular Lens Replacement Surgery

NCT02093689

Phase 3 Terminated 18 enrolled Omeros Corporation
Non-randomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the effect of OMS302 on the signs of Intraoperative Floppy Iris Syndrome in patients at risk.

Timeline

Start
2014-02
Primary completion
2014-08
Completion
2014-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketorolac Other / unclassified 4.24 mg/ml Other
Subject Phenylephrine Small molecule 12.37 mg/ml Other