Collecting data on pupillometer assessments in neuro-intensive care

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to gather extensive data on pupillometer readings to establish normative values for pupillary assessments in critically ill patients. By collecting data from patients in intensive care units who undergo regular pupillary evaluations, the study seeks to enhance understanding of clinically relevant pupil metrics such as size, reactivity, and the neurological pupil index. The data collected will serve as a foundation for future research and improve the interpretation of pupillary assessments in critical care settings.

Why it matters

Who can join: the full rules

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

Where it's running

• Maria E Denbow
  Dallas, Texas, United States Recruiting

Study contacts

• Study coordinator: DaiWai M Olson, PhD
• Email: DaiWai.Olson@UTSouthwestern.edu
• Phone: 214-648-8946

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.