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Clinical Trial Summary

Intraoperative floppy iris syndrome (IFIS) is a recently described condition observed during cataract surgery. It has been hypothesized that irreversible atrophy of the iris dilator muscle associated with α1-adrenergic receptor antagonists (α1-ARA) is responsible for IFIS. However the prevalence of IFIS in Korean population is not reported. The purpose of this study is to evaluate the prevalence and clinical manifestations of IFIS in relation to iris anatomical change in Korean patients taking α1-ARA.


Clinical Trial Description

n/a


Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Intraoperative Floppy Iris Syndrome
  • Syndrome

NCT number NCT01704014
Study type Observational
Source Samsung Medical Center
Contact
Status Completed
Phase N/A
Start date January 2010
Completion date March 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
Terminated NCT02093689 - Intraoperative Floppy Iris Syndrome Undergoing Intraocular Lens Replacement Surgery Phase 3
Terminated NCT00627913 - Retrobulbar Injection of Anesthesia Versus Healon 5 in the Management of Intraoperative Floppy Iris Syndrome N/A