Status:
COMPLETED
Effects of Sevoflurane and Propofol on Light Flashed Evoked Pupillometry
Lead Sponsor:
Rutgers, The State University of New Jersey
Conditions:
Blindness
Eligibility:
All Genders
18-70 years
Brief Summary
This is a study to focus on the feasibility of using a monitor which may signal loss of visual function intraoperatively.
Detailed Description
The degree of a relative afferent pupillary defect (RAPD) has been correlated with the severity of an eye injury and has been shown to have prognostic significance as an indicator of retinal ischemia....
Eligibility Criteria
Inclusion
- planned orthopedic surgery on the lower extremities and positioned on the back
Exclusion
- recent bout of conjunctivitis or pink eye
- condition which inhibits the normal pupillary function of my eye
Key Trial Info
Start Date :
August 1 2007
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 1 2010
Estimated Enrollment :
35 Patients enrolled
Trial Details
Trial ID
NCT01219569
Start Date
August 1 2007
End Date
January 1 2010
Last Update
April 24 2015
Active Locations (1)
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1
University Hospital
Newark, New Jersey, United States, 07101