Establishing Normative Data for Pupillometer Assessments in Neuro-Intensive Care
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorUniversity of Texas Southwestern Medical Center
About this trial
The purpose of this study is to collect a large amount of data that may assist in addressing the gap in knowledge of understanding pupillometer readings using a pupillometer device.
The aim of this project is to establish normative values for pupillometer data. Measures of central tendency will be developed for the variables provided by automated pupillary exams, which will provide an enhanced understanding of clinically appropriate pupil values for size, reactivity, and neurological pupil index.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Data will be collected on patients admitted to enrolling hospitals who have been assigned, by the attending physician, to have regular pupillary assessments, and in whom staff nurses are performing pupillary assessments with the pupillometer.
Disqualifiers
Out-patients
Patients that do not have orders for regular pupillary assessments
Trial population
In-patient
Trial design
Design model
Other
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Oculomotor evaluation of pupillary variance during ICU admission
Pupil size and reactivity per neurological pupil index
Time frame
Daily at 9:00amSponsors and contacts
Click on the lead sponsor to view all of their trials.
University of Texas Southwestern Medical Center
Lead sponsor
NeurOptics Inc
Collaborator
Source ClinicalTrials.gov