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MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care

NCT00400062 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 800

Last updated 2019-04-19

No results posted yet for this study

Summary

This will be the first large cohort study to define the epidemiology of and identify modifiable risk factors for long-term CI and functional deficits of ICU survivors. The investigators will measure the independent contribution of risk factors such as delirium and exposure to sedative and analgesic medications to the incidence of long-term CI, controlling for established risk factors (e.g., age, pre-existing CI, and apoE genotype). Defining the contributions of these risk factors will make it possible to develop preventive and/or treatment strategies to reduce the incidence, severity and/or duration of long-term CI and improve functional recovery of patients with acute critical illness.

Conditions

Sponsors & Collaborators

  • Vanderbilt University Medical Center

    collaborator OTHER

  • VA Office of Research and Development

    lead FED

Principal Investigators

  • E. Wesley Ely, MD MPH · Tennessee Valley Healthcare System Nashville Campus, Nashville, TN

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-07-01
Primary Completion
2010-12-01
Completion
2017-12-01

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00400062 on ClinicalTrials.gov