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Clinical Trial Summary

In this study, the investigators plan to compare the incidence and complications of intraoperative floppy iris syndrome (IFIS) during cataract surgery in patients taking tamsulosin (Flomax) and treated with retrobulbar injection of anesthesia, versus injection of Healon 5 viscoelastic into the anterior chamber.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Intraoperative Floppy Iris Syndrome
  • Syndrome

NCT number NCT00627913
Study type Interventional
Source Penn State University
Contact
Status Terminated
Phase N/A
Start date February 2008
Completion date November 11, 2010

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 NCT02093689 - Intraoperative Floppy Iris Syndrome Undergoing Intraocular Lens Replacement Surgery Phase 3