Interventions for Postoperative Delirium: Biomarker-3

Part of paid clinical trials in Madison, Wisconsin.

Sponsor
University of Wisconsin, Madison
Study ID
NCT03124303
Status
Recruiting
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Conditions

  • Delirium

Eligibility Criteria

Sex
ALL
Age
60 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • High Density-Electroencephalogram — PROCEDURE
    EEG is a safe non-invasive technology without complications that may be used to help diagnose delirium
  • Magnetic Resonance Imaging — PROCEDURE
    MRI scan of brain
  • Blood specimen collection — PROCEDURE
    Blood will be collected from participants
  • Pupillometry — DIAGNOSTIC_TEST
    A pupillometer is a device that measures the size of the pupils.

Study Details

The IPOD-B3 study aims to characterize the relationship between premorbid brain activity and postoperative delirium in patients undergoing major surgery. This is a expansion of the NeuroVISION Bolt-On study, NCT01980511.

Key Dates

First listed
Apr 21, 2017
Start date
Feb 13, 2017
Status verified
Dec 2025
Primary completion
Dec 31, 2029
Completion
Dec 31, 2029

Study Design

Enrollment
468 participants (estimated)

Arms

  • Arm: Participants 1-320
    First 320 participants enrolled
  • Arm: Participants 321-470
    Final 150 participants enrolled

Primary Outcome Measure

Functional Connectivity [ Time Frame: Pre-operative measure: Up to 4 weeks prior to surgery. Post-operative measure: Post-Operative days 1-4 ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of Wisconsin-MadisonMadisonWisconsin53792
David Kunkel, BS
[email protected]
608-262-6469
Frankie Ingram, BS
[email protected]
608-262-6469
Robert Pearce, MD PhD (PRINCIPAL_INVESTIGATOR)

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By research site
University of Wisconsin-Madison· Madison, WI

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