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RECRUITING NA

Delirium and Neuropsychological Recovery Among Emergency General Surgery Survivors

NCT05373017 · View on ClinicalTrials.gov ↗

Study Summary

This study will evaluate the usefulness of the Urgent and Emergency Surgery (UES) Delirium Recovery Model. It is hypothesized that the cognitive, physical and psychological recovery of older UES delirium survivors will be improved through the use of the DANE Recovery Model. Participants can expect to be on the study for 18 months.

Conditions Studied

Interventions

  • OTHER Questionnaires
  • OTHER DANE Recovery Program

Study Locations (6)

Wisconsin

  • University of Wisconsin — Madison
  • Meriter Hospital — Madison
  • East Madison Hospital — Madison
  • Medical College of Wisconsin — Milwaukee

Illinois

  • SwedishAmerican Hospital — Rockford

Indiana

  • Indiana University — Indianapolis

Trial Details

FieldValue
Enrollment Target 528 participants
Start Date 2023-02-13
Est. Completion 2027-06-30
Phase NA

Sponsor

University of Wisconsin, Madison

943 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05373017

The ClinicalTrials.gov registry entry for NCT05373017 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 528 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Wisconsin, Madison, which has 943 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Delirium appearing as the primary indexed condition, and to 2 interventions — of which Questionnaires is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05373017 reports 6 study locations spanning 3 distinct geographic areas — top geographies include Wisconsin, Illinois, Indiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05373017 about?

NCT05373017 is a clinical study titled "Delirium and Neuropsychological Recovery Among Emergency General Surgery Survivors". This study will evaluate the usefulness of the Urgent and Emergency Surgery (UES) Delirium Recovery Model. It is hypothesized that the cognitive, physical and psychological recovery of older UES delirium survivors will be improved through the use of the DANE Recovery Model. Participants can expect t...

What is the current status of trial NCT05373017?

This trial is currently recruiting. It is a NA study. The enrollment target is 528 participants. The study started on 2023-02-13. Estimated completion is 2027-06-30.

What conditions does trial NCT05373017 study?

This clinical trial studies the following conditions: Delirium. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05373017?

The interventions under investigation include: Questionnaires (OTHER), DANE Recovery Program (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05373017?

This trial is sponsored by University of Wisconsin, Madison, which has 943 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05373017 being conducted?

This trial has 6 study locations across Illinois, Indiana, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial