Effects of Sevoflurane and Propofol on Light Flashed Evoked Pupillometry

Completed

Conditions studied: Blindness

In brief

This is a study to focus on the feasibility of using a monitor which may signal loss of visual function intraoperatively.

Key facts

Study ID

NCT01219569

Run by

Rutgers, The State University of New Jersey

People needed

35

Starts

2007-08-01

Expected to finish

2010-01-01

Last updated by the study team

2015-04-24

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• planned orthopedic surgery on the lower extremities and positioned on the back

You may not qualify if…

• recent bout of conjunctivitis or pink eye
• condition which inhibits the normal pupillary function of my eye

Where it is running

• University Hospital — Newark, New Jersey, United States

Full record on ClinicalTrials.gov

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