PACU Discharge Readiness

Starting soon · Not applicable

Conditions studied: Patient Discharge, Neurocognition, Baseline

In brief

The use of custom-created apps, neuropsychological testing, and clinical assessments will be evaluated as tools for determining the appropriateness of PACU discharge to home.

Key facts

Study ID

NCT07588542

Run by

University of Illinois at Chicago

People needed

1000

Starts

2026-05-01

Expected to finish

2032-04-01

Last updated by the study team

2026-05-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The individuals will be identified from the operating room (OR) schedule and approached in the pre-operative area (or earlier, when possible).
• Adult patients (18 years or older) listed for surgery and a planned 23-hour admission will be eligible for enrollment in this study.
• Subjects must be fluent in English and not have confounding sensory or neurological limitations to participation

You may not qualify if…

• Members of vulnerable populations or adults unable to consent will be included in this study.
• Subjects that do not speak English
• Subjects with neurological limirations

Where it is running

• University of Illinois Chicago — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

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