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Completed

NCT Number: NCT03098472

Cholinesterase Activity and DeliriUm During Critical Illness Study

Delirium is a syndrome of acute brain dysfunction involving attention and cognition that affects up to half of older hospitalized patients and 50%-75% of critically ill ICU patients, such that millions of patients worldwide experience this acute threat to their health and well being every year. One-third to half of critical illness survivors struggle with a dementia-like disorder similar in severity to moderate-to-severe traumatic brain injury or Alzheimer's Disease, and the only proven risk factor that is potentially modifiable is delirium in the ICU. Despite the frequency and impact of delirium in the ICU, little is known regarding the biological mechanisms that lead to this form of organ dysfunction during critical illness. A widely held hypothesis proposes that inflammation is regulated by the cholinergic system, and that this interaction plays a pivotal role whether delirium developments in the setting of acute illness. Acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) are enzymes that hydrolyze the neurotransmitter acetylcholine. Changes in the activity of these enzymes, which can be measured in whole blood, reflect altered regulation of circulating acetylcholine. AChE and BuChE activities have promise as both predictors of delirium (when found to be low at admission) and biomarkers of delirium (when low during serial measurement). Neither of these biomarkers, however, have been studied in the ICU setting where delirium risk is the highest. The current investigation, therefore will be the first to determine the validity of circulating AChE and BuChE activities as biomarkers of delirium during critical illness and subsequent cognitive impairment after discharge. This study will measure whole blood AChE and butyrylcholinesterase BuChE activities within the framework of the ICU Delirium and Cognitive Impairment Study Group's ongoing clinical trials in critically ill patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Vanderbilt University Medical Center

Nashville, Tennessee, 37212, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • English-speaking adults (>18 years of age) treated for acute respiratory failure (with mechanical ventilation or non-invasive positive pressure ventilation [NIPPV]) and/or shock (with vasopressors) in a medical and/or surgical ICU at Vanderbilt University Medical Center enrolled in an ICU Delirium and Cognitive Impairment Study Group's clinical trials. Exclusion criteria for the parent studies are summarized below. No additional exclusion criteria are required for this investigation.

Exclusion criteria

  • Expected death within 24 hours of enrollment or lack of commitment to aggressive treatment by family or the medical team (e.g., likely withdrawal of life support measures within 24 hours of screening)
  • Active substance abuse, psychotic disorder, or homelessness without a secondary contact person (which would make long-term follow-up difficult)
  • Blindness or deafness (which would prevent assessment of the study's outcomes)
  • Inability to obtain informed consent

Treatment and study plan

Primary outcomes

  1. Delirium

    Time frame: During hospital stay until death or hospital discharge, whichever comes first, up to 30 days

    Confusion Assessment Method for the ICU

Secondary outcomes

  1. Global cognition

    Time frame: At 3, 6, and/or 12 months after hospital discharge up to 18 months after discharge

    Neuropsychological battery

Other outcomes

  1. Activities of daily living

    Time frame: At 3, 6, and/or 12 months after hospital discharge up to 18 months after discharge

    Katz Index of Independence in Activities of Daily Living

  2. Instrumental activities of daily living

    Time frame: At 3, 6, and/or 12 months after hospital discharge up to 18 months after discharge

    Functional activities questionnaire

  3. Quality of life and generic health status

    Time frame: At 3, 6, and/or 12 months after hospital discharge up to 18 months after discharge

    EQ-5D

  4. Coma

    Time frame: During hospital stay until death or hospital discharge, whichever comes first, up to 30 days

    Richmond Agitation Sedation Scale

Sponsors and collaborators

Lead sponsor

Vanderbilt University Medical Center

Other

Collaborators

  • DR. FRANZ KOHLER CHEMIE GMBH

Registry information

Acronym: CADUCeuS

Important dates

Study start
2017
Primary completion
2020
Study completion
2021
First posted
Mar 31, 2017
Registry last updated
Mar 11, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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