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Delirium clinical trials

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NCT ID: NCT00991913 Completed - Delirium Clinical Trials

Risk Factors of Recovery Room Delirium After Elective Non-cardiovascular Surgery

Start date: June 1, 2010
Phase:
Study type: Observational

Despite recent advances in postoperative delirium research, the proportion of patients with postoperative delirium is still high ranging between 20-80%. Although postoperative delirium is a frequent complication and is associated with the need for more inpatient hospital care and longer length of hospital stay, little is known about risk factors for recovery room delirium (RRD) occurred in postanaesthesia care unit. The aim of the study was to determine pre- and intraoperative risk factors for the development of RRD among patients undergoing non cardiovascular surgery.

NCT ID: NCT00991328 Terminated - Clinical trials for Postoperative Cognitive Dysfunction

Role of Absolute Cerebral Oximetry to Prevent Neurocognitive Injury in Elderly Patients Undergoing Cardiac Surgery

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether brain oxygenation measured by cerebral oximeter has an impact on neurocognitive dysfunction.

NCT ID: NCT00961389 Unknown status - Delirium Clinical Trials

Validating a Delirium Prediction Model for Critically Ill Patients

Start date: May 2009
Phase: N/A
Study type: Observational

The objective of this study is to determine the incidence of delirium in adults patients who are admitted at the critical care unit of a Dutch University Hospital with the mapping of relevant delirium risk factors The primary aim is to validate the investigators' developed delirium prediction model for critical care patients. A secondary aim is to find differences between delirious patients and non-delirious patients on different aspects of diagnostics, treatment and care, outcome, length of stay, and inflammation. According to Dutch law, the need to obtain informed consent was waived by the Committee on Research Involving Human Subjects (CMO) of Nijmegen for this observational study (2007/283).

NCT ID: NCT00954603 Terminated - Delirium Clinical Trials

A Double-blind, Randomized, Controlled Trial of Quetiapine Versus Haloperidol for the Treatment of Delirium

QHdelirium
Start date: June 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether quetiapine, and haloperidol are effective and safe in the treatment psychiatric symptoms in patients with delirium.

NCT ID: NCT00919698 Completed - Delirium Clinical Trials

Delirium in Mechanically Ventilated Patients

Start date: June 2010
Phase: N/A
Study type: Observational

The overall purpose of this trial is to assess the relationship between a daily awakening from sedation and the prevalence of delirium, and in doing so better characterize delirium in the ICU.

NCT ID: NCT00911677 Completed - Delirium Clinical Trials

Does APOE-e4 Predict Delirium and Cognitive Dysfunction After Surgery?

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

Patients with the APOE-ε4 genotype are at increased risk of both vascular dementia and peripheral vascular disease. Patients undergoing major vascular surgery are at particularly high risk of delirium and other, more subtle, changes in cognitive function following surgery. The hypothesis of this trial is that the APOE-ε4 genotype is associated with both delirium and postoperative cognitive dysfunction (POCD).

NCT ID: NCT00885443 Completed - Emergence Delirium Clinical Trials

Emergence Delirium in Children: Total Intravenous Anesthesia With Propofol and Remifentanil Versus Inhalational Sevoflurane Anesthesia

Start date: February 2009
Phase: N/A
Study type: Interventional

Emergence delirium (ED) refers to a wide variety of behavioural disturbances that are commonly seen in children following emergence from anesthesia. ED can potentially be dangerous and have serious consequences for the child such as injury, increased pain, and dislodgement of medical devices, often requiring physical restraint or pharmacological control. Witnessing this behaviour can be stressful for parents, which can negatively affect their interaction with the healthcare system, and their relationship with the child, nursing staff and other healthcare providers. The investigators aim to minimize ED to reduce the distress experienced by patients and their parents. This study will compare the recovery profile of sevoflurane with that of propofol remifentanil and their associated incidence of ED. This study should enable us to determine which form of anesthesia is associated with the fewest incidences of ED in children.

NCT ID: NCT00873379 Completed - Delirium Clinical Trials

Melatonin Supplementation for Delirium Prevention in Acutely Hospitalized Elderly

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

122 people over 70 who were admitted to hospital were enrolled to the study. Half got .5 mg a night of melatonin, half got a placebo.

NCT ID: NCT00865202 Completed - Clinical trials for Post-operative Delirium

A Placebo Controlled Trial Of L-Tryptophan In Post-Operative Delirium

Start date: December 2008
Phase: Phase 3
Study type: Interventional

Post-operative delirium is a common and deleterious complication in elderly patients. The investigators have previously found lower levels of serum tryptophan in post-operative elderly patients who developed delirium in comparison to post-operative elderly patients who did not develop delirium. The investigators hypothesize that post-operative supplementation of L-tryptophan will reduce the duration and incidence of post-operative delirium. This study is a double-blinded placebo controlled trial of L-tryptophan supplementation in post-operative ICU patients 60 years and older. The primary outcome measure is the comparison of duration of post-operative delirium in subjects who receive L-tryptophan supplementation versus a similar appearing control.

NCT ID: NCT00857727 Completed - Anesthesia Clinical Trials

Use of Dexmedetomidine to Reduce Emergence Delirium Incident in Children

DexPeds
Start date: August 2009
Phase: Phase 3
Study type: Interventional

Emergence delirium (ED) from general anesthesia posts risk and harm to pediatric population undergo general anesthesia. The purpose of the study is to compare the use of dexmedetomidine versus placebo in reducing the incidence and severity of ED in a pediatric neurosurgical population.