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Establishing Normative Data for Pupillometer Assessments in Neuro-Intensive Care

Establishing Normative Data for Pupillometer Assessments in Neuro-Intensive Care

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02804438
Acronym
ENDPANIC
Enrollment
1000
Registered
2016-06-17
Start date
2015-07-31
Completion date
2028-09-30
Last updated
2025-10-22

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

Conditions

Critical Illness, Neuropathy

Brief summary

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.

Detailed description

Data will be collected on patients in the intensive care units at the selected hospitals on patients 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. While a sample size estimate would be considered inappropriate for registry development, power analysis techniques were used to examine the potential of this registry to generate adequate information to begin to fully describe normative data for pupillary exams. Using the assumption that the desire is to understand neurological pupil index (NPi) and size differences within 0.1, and that the spread of data would be approximately normally distributed, a minimum of 3,250 observations is required (alpha = 0.05, beta = 0.80). It must, however, be repeated that this is simply a rough estimate. The registry data generated will, in fact, be the source of data from which future studies will be powered.

Interventions

None listed

Sponsors

NeurOptics Inc.
CollaboratorINDUSTRY
University of Texas Southwestern Medical Center
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* Out-patients * Patients that do not have orders for regular pupillary assessments

Design outcomes

Primary

MeasureTime frameDescription
Oculomotor evaluation of pupillary variance during ICU admissionDaily at 9:00amPupil size and reactivity per neurological pupil index

Countries

United States

Contacts

Primary ContactDaiWai M Olson, PhD
DaiWai.Olson@UTSouthwestern.edu214-648-8946
Backup ContactMaria E Denbow
Maria.Denbow@utsouthwestern.edu214-648-2861

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026