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Clinical Trial 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.


Clinical Trial Description

OMS302 is a mydriatic/anti-inflammatory combination investigational drug product being developed for use during intraoperative lens replacement (ILR). This study evaluates the effect of OMS302 on the signs of Floppy Iris Syndrome in subjects with a history of tamsulosin exposure who are undergoing ILR. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02093689
Study type Interventional
Source Omeros Corporation
Contact
Status Terminated
Phase Phase 3
Start date February 2014
Completion date August 2014

See also
  Status Clinical Trial Phase
Completed NCT01693575 - Use of APX 100 Device for Small-pupil Cataract Surgery and Intraoperative Floppy-iris Syndrome N/A
Recruiting NCT01070602 - The Effect of Anterior Corneal Incisions on Intraoperative Floppy Iris Syndrome (IFIS) Incidence and Severity in Tamsulosin Treated Cataract Patients N/A
Completed NCT06266962 - Comparing the Efficiency of Two Approaches in Patients at Risk of Developing Intraoperative Floppy Iris Syndrome Phase 4
Completed NCT03760185 - Pupil Dilation for Treatment of IFIS Phase 2
Completed NCT01704014 - Intraoperative Floppy Iris Syndrome in Korean Patients Taking α1-Adrenergic Receptor Antagonists N/A
Terminated NCT00627913 - Retrobulbar Injection of Anesthesia Versus Healon 5 in the Management of Intraoperative Floppy Iris Syndrome N/A