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Establishing Normative Data for Pupillometer Assessments in Neuro-Intensive Care (ENDPANIC)

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Enrolling

Conditions

Critical Illness
Neuropathy

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT02804438
STU 062015-005

Details and patient eligibility

About

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.

Full 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.

Enrollment

1,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Central trial contact

DaiWai M Olson, PhD; Maria E Denbow

Data sourced from clinicaltrials.gov

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