Clinical Trials Directory

Trials / Completed

CompletedNCT00472888

Clinical Factors Associated Floppy Iris

Clinical Factors Associated With Floppy Iris Signs: a Prospective Study From Two Centers

Status
Completed
Phase
Study type
Observational
Enrollment
500 (actual)
Sponsor
Baskent University · Academic / Other
Sex
All
Age
28 Years – 90 Years
Healthy volunteers
Accepted

Summary

This study is planned to investigate the incidence of intraoperative floppy iris and its relationship with pseudoexfoliation, diabetes, hypertension as well as systemic alpha-1 adrenergic blocker use.

Detailed description

Our aim is to investigate the incidence of intraoperative floppy iris syndrome (IFIS) signs and evaluate the relationship of IFIS signs as well as complete IFIS with pseudoexfoliation, diabetes, hypertension, and alpha-1 adrenergic blocker (A1AB) use. Five-hundred patients will be included in this prospective study. Preoperatively, pupil diameter before and after dilation, presence of pseudoexfoliation, history of diabetes, hypertension, and use of any A1AB will be recorded. Intraoperative adverse events such as pupillary constriction, iris billowing, and iris prolapse from the wound will be noted. Multinomial regression analysis will be used to evaluate the relationship of IFIS signs with pseudoexfoliation, diabetes, hypertension, and A1AB usage. According to the results we will determine the incidence of IFIS in our patient population and evaluate its relationship with alpha-1 adrenergic blocker use. We will also investigate the relationship of floppy iris problems with pseudoexfoliation, diabetes, high blood pressure.

Conditions

Timeline

Start date
2005-11-01
Completion
2006-11-01
First posted
2007-05-14
Last updated
2007-05-14

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT00472888. Inclusion in this directory is not an endorsement.