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Delirium clinical trials

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NCT ID: NCT00564434 Completed - Delirium Clinical Trials

Postoperative Delirium in Hip Fracture Patients

Start date: May 2005
Phase: N/A
Study type: Observational

Risk factors for postoperative delirium in hip fracture patients.

NCT ID: NCT00561678 Completed - Clinical trials for Postoperative Delirium

Perioperative Cognitive Function - Dexmedetomidine and Cognitive Reserve

Start date: February 2008
Phase: Phase 4
Study type: Interventional

Elderly patients who undergo anesthesia and non-cardiac surgery are subject to deterioration of brain function including the development of postoperative delirium (PD) and postoperative cognitive dysfunction (POCD). These disorders cause disability, distress for both patients and their families, are associated with other medical complications and account for significant additional health care costs. We currently use relatively primitive approaches to preventing and treating PD and POCD. Dexmedetomidine is a drug used for sedation in critically ill patients that provides some pain relief and controls the bodies response to stress. The sedation produced by dexmedetomidine appears more similar to natural sleep than any other drug used for anesthesia and postoperative sedation. Data suggesting that dexmedetomidine can prevent delirium following cardiac surgery and the developing understanding of the causes of PD and POCD suggest that dexmedetomidine will be particularly effective.

NCT ID: NCT00533884 Completed - Lung Cancer Clinical Trials

Neurocognitive Functioning in Patients With Newly Diagnosed Upper Aerodigestive Tract Cancer Receiving Treatment at Henry-Joyce Cancer Clinic

Start date: October 2007
Phase: N/A
Study type: Observational

RATIONALE: Gathering information about how often problems with neurocognitive functioning occur in patients with newly diagnosed upper aerodigestive tract cancers may help doctors learn more about the disease. PURPOSE: This clinical trial is studying neurocognitive functioning in patients with newly diagnosed upper aerodigestive tract cancers receiving treatment at Henry-Joyce Cancer Clinic.

NCT ID: NCT00512291 Completed - Advanced Cancer Clinical Trials

Subcutaneous Olanzapine for Hyperactive or Mixed Delirium

Start date: June 2005
Phase: N/A
Study type: Interventional

The objective of this study is to determine the tolerability and safety of olanzapine administered as a subcutaneous injection to hospitalized patients with hyperactive or mixed delirium.

NCT ID: NCT00507481 Completed - Delirium Clinical Trials

Evaluation of Risk Factors of Sleep Quality in Intensive Care Unit

Start date: January 2006
Phase: N/A
Study type: Observational

The aim of this study was to investigate the relationship between sleep disturbances and delirium in surgical ICU patients. The study set up to test the hypothesis that the occurrence of delirium is associated to the alteration of sleep quality and quantity observed in the critically ill patients.

NCT ID: NCT00505804 Completed - Delirium Clinical Trials

A Comparison of Dexmedetomidine and Haloperidol in Patients With Intensive Care Unit (ICU)-Associated Agitation and Delirium

Dex
Start date: January 2005
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine whether dexmedetomidine is a more effective medication than haloperidol in the treatment of agitation and delirium in patients receiving mechanical ventilation in an intensive care unit. Haloperidol is a medication conventionally used for this purpose. The investigators will study only patients who have recovered from their illness to the point that, were it not for agitation and delirium, they would no longer require mechanical ventilation. The investigators hypothesize that patients receiving dexmedetomidine will be able to discontinue mechanical ventilation earlier than those receiving haloperidol.

NCT ID: NCT00493714 Completed - Advanced Cancer Clinical Trials

Delirium Recall in Advanced Cancer Patients

Start date: July 2005
Phase: N/A
Study type: Observational

Primary Objectives: 1. To determine the proportion of patients who experience partial or complete recollection of symptoms of delirium and the level of distress associated with this recall. 2. To determine caregiver's level of distress associated with the patient's episode of delirium.

NCT ID: NCT00469482 Completed - Clinical trials for Cognitive Impairment

The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status

SOMNUS
Start date: June 2007
Phase: N/A
Study type: Interventional

A combined strategy of Richmond Agitation and Sedation Scale (RASS) clinical targeting plus bispectral index (BIS) guided sedation in mechanically ventilated, critically ill patients will decrease time on mechanical ventilation, decrease the duration of intensive care unit (ICU) delirium and coma, and will improve subacute neurocognitive function when compared to sedation guided by RASS targeting alone.

NCT ID: NCT00464763 Withdrawn - Delirium Clinical Trials

A Research Study to Evaluate the Effectiveness of Dexmedetomidine in Preventing Delirium After Heart Surgery

Start date: April 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of dexmedetomidine in the prevention of postoperative delirium in subjects undergoing heart valve surgery with or without coronary artery bypass surgery (CABG) using cardiopulmonary bypass (CPB).

NCT ID: NCT00463333 Completed - Clinical trials for Postoperative Delirium

Postoperative Delirium at Heidelberg's Intensive Care Unit -New Diagnostic Markers

Start date: May 2005
Phase: N/A
Study type: Observational

Summary: Postoperative delirium is a highly prevalent disease (10–30% prevalence) after surgery in intensive care unit, however, it is often misdiagnosed and mistreated. The aim of the present project is to investigate risk factors for postoperative delirium in more detail, to evaluate respective cognitive test systems and to measure EEG activity parallel to patients’ serum anticholinergic activity. The pathophysiology of delirium is unknown up to now: a possible dysbalance between cerebral acetylcholine and dopamine concentrations is a likely hypothesis. Therefore, the measurement of peripheral serum anticholinergic activity could be a new prognostic factor for evaluation of delirium. Because delirium is also associated with higher postoperative mortality and morbidity, with delayed functional recovery, and postoperative delirium makes patient management much more difficult, increases costs, and, above all, causes severe discomfort to the patient new interdisciplinary diagnostic strategies are necessary to resolve this problem.