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NCT00096863 · ClinicalTrials.gov registry record · Phase 2

The MIND Study: Modifying the INcidence of Delirium

A Phase 2 study, sponsored by Vanderbilt University.

Completed
Registry status
Phase 2
Development phase
102
Enrollment target

NCT00096863 is a Phase 2 study that has completed, run by Vanderbilt University. The registered enrollment target is 102 participants.

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The verdict

NCT00096863, a Phase 2 study, has completed, sponsored by Vanderbilt University.

COMPLETED
Registry status
Phase 2
Development phase
102 participants
Enrollment target

Study Summary

Delirium is associated with increased risk of death, prolonged stay, higher cost of care, and likely long-term brain deficits in survivors. This form of brain dysfunction occurs in intensive care unit (ICU) patients in epidemic proportions, and the scope of this problem is likely to worsen in upcoming years due to the aging of our population and increased utilization of the ICU. Currently, delirium goes unrecognized and untreated in the vast majority of circumstances in the ICU unless the patient presents with hyperactive delirium and agitation. In the latter circumstance, a commonly used typical antipsychotic called haloperidol is considered the principal agent for treating delirium based largely on anecdotal evidence to support its usefulness, though no placebo controlled trials exist. There are no FDA approved medications for delirium. The atypical antipsychotics provide a promising alternative for the treatment of delirium due to their enhanced beneficial effects on positive (agitated) and negative (quiet) symptoms proven in mania and schizophrenia, reduced risk for side effects common to haloperidol such as extrapyramidal symptomatology, and less potentially lethal heart rhythm disturbances. It is imperative that well-designed phase II studies to determine proof of principle be conducted. A pilot study of feasibility to begin assessing the role of antipsychotics in the management of ICU delirium.

Interventions

  • OTHER Placebo
  • DRUG Haloperidol
  • DRUG Ziprasidone

Trial Details

FieldValue
Enrollment Target 102 participants
Start Date 2004-12
Est. Completion 2007-07
Phase Phase 2

Sponsor

Vanderbilt University

430 total trials

What the Registry Record Tells You About NCT00096863

The ClinicalTrials.gov registry entry for NCT00096863 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 102 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University, which has 430 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT00096863 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00096863 about?

NCT00096863 is a clinical study titled "The MIND Study: Modifying the INcidence of Delirium". Delirium is associated with increased risk of death, prolonged stay, higher cost of care, and likely long-term brain deficits in survivors. This form of brain dysfunction occurs in intensive care unit (ICU) patients in epidemic proportions, and the scope of this problem is likely to worsen in upcomi...

What is the current status of trial NCT00096863?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 102 participants. The study started on 2004-12. Estimated completion is 2007-07.

What interventions are being tested in trial NCT00096863?

The interventions under investigation include: Placebo (OTHER), Haloperidol (DRUG), Ziprasidone (DRUG).

Who is sponsoring clinical trial NCT00096863?

This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.

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

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