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Effects of Sevoflurane and Propofol on Light Flashed Evoked Pupillometry

The Effects of Sevoflurane and Propofol on Light Flashed Evoked Pupillometry

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01219569
Enrollment
35
Registered
2010-10-13
Start date
2007-08-31
Completion date
2010-01-31
Last updated
2015-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blindness

Keywords

blindness, ischemic optic neuropathy

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. Therefore light flashed evoked pupillometry (LFEP) may serve as a useful indicator of visual function. LFEP's are not known to be sensitive to anesthetics. We will measure LFEP's using different anesthetic techniques to see if there are measurable differences in the latency, amplitude and constriction velocity of the pupillary reflex. Prior to induction of anesthesia, pupillometer readings will be taken in the supine position in both eyes. The patient will be anesthetised using a standard induction technique. For maintenance of anesthesia a remifentanil infusion will be administered and supplemented by either propofol infusion (at 120 and 160 mcg/kg/min)or sevoflurane (at 1.5 and 2.5% end-tidal in random sequence. The patients will receive muscle relaxants as needed. Pupillometry readings will be taken in both eyes after induction, after steady maintenance has been achieved and every 10 minutes for 30 minutes at each drug dose.

Interventions

DRUGpropofol

Propofol infusion 120 and 160 mcg/kg/min in random sequence during the operative procedure

DRUGSevoflurane

sevoflurane 1.5% and 2.5% end tidal in random sequence

Sponsors

Rutgers, The State University of New Jersey
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Measure the pupil response using different anesthetic techniquespupillometry measurements will be taken in both eyes after induction of anesthesia

Secondary

MeasureTime frame
Measure the pupil response using different anesthetic techniquesWhen steady maintenance of anesthesia drug is obtained measure pupillometry response at 10 min
Measure the pupil response using different anesthetic techniqueWhen steady maintenance of anesthesia drug is obtained measure pu[illometry response at 30 minutes.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026