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Delirium clinical trials

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NCT ID: NCT03486288 Terminated - Clinical trials for Cognitive Impairment

Cognitive Impairment Following Elective Spine Surgery

CONFESS
Start date: February 6, 2018
Phase:
Study type: Observational

Older people are a rapidly growing proportion of the world's population and their number is expected to increase twofold by 2050. When these people become patients that require surgery, they are at particular high risk for postoperative delirium (POD), which is associated with longer hospital stays, higher costs, risk for delayed complications and cognitive dysfunction (POCD). Having suffered an episode of delirium is furthermore a predictor of long-term care dependency. Despite these risks, an increasing number of elderly undergo major elective surgery. This is reflected by the frequency of elective spinal surgery, in general, and instrumented fusions, in particular, which has markedly increased over the past few decades. It is yet insufficiently understood, which, particularly modifiable, factors contribute to the development of POD and POCD following these major but plannable surgeries. A better understanding of risk factors would facilitate informed patient decisions and surgical strategies could be tailored to individual risk profiles.

NCT ID: NCT03342989 Terminated - Dementia Clinical Trials

Speed of Processing Training for Cognitive Deficits After Delirium in Older Adults

Start date: August 13, 2018
Phase: N/A
Study type: Interventional

In this proposal, we will examine processing speed training (PST) as a potential intervention to reduce the risk of developing long-term cognitive impairment after a delirium episode.

NCT ID: NCT03337282 Terminated - Clinical trials for Cognitive Impairment

Incidence and Characteristics of Postoperative Cognitive Dysfunction in Elderly Quebec Francophone Patients

Start date: September 21, 2017
Phase:
Study type: Observational

The purpose of this study is to determine what percentage of patients have cognitive problems (for example, memory or concentration difficulties) after surgery and anesthesia, what the characteristics of these problems are, and whether they persist over time. In particular, the investigators want to study this in the French-speaking Quebec population with cognitive evaluation tools adapted for this population.

NCT ID: NCT03212300 Terminated - Clinical trials for Postoperative Delirium and Delayed Functional Recovery

TSA Exercise Prehabilitation in Older Adults

Start date: September 28, 2018
Phase: N/A
Study type: Interventional

This is a randomized study to examine whether aerobic exercise training (AET) before total shoulder replacement (TSR) surgery reduces the incidence of post-operative delirium (POD) and shorten time to recovery in elderly patients. POD is a form of sudden change in mental function that can be experienced after undergoing surgery.

NCT ID: NCT03200600 Terminated - Clinical trials for Carcinoma, Non-Small-Cell Lung

Dexamethasone, Flurbiprofen Axetil and Delirium After Lung Cancer Surgery

Start date: August 2, 2017
Phase: Phase 4
Study type: Interventional

Delirium is a common complication in elderly patients after surgery. And its occurrence is associated with worse outcomes. The causes of delirium are multifactorial but may include pain, stress response and inflammation. Dexamethasone is commonly used to prevent the occurrence of postoperative nausea and vomiting. In a randomized controlled trial, small-dose dexamethasone (8 mg) administered before anesthesia induction improved the quality of recovery in patients after cardiac surgery. Flurbiprofen axetil is commonly used to improve postoperative analgesia while decreasing the requirement of opioids. In a randomized trial of the investigators, combined use of flurbiprofen axetil with sufentanil for postoperative analgesia reduced delirium in elderly patients after orthopedic surgery. The purpose of this 2 plus 2 factorial randomized controlled trial is to test the hypothesis that combined use of dexamethasone and flurbiprofen axetil may reduce delirium in elderly patients after lung cancer surgery.

NCT ID: NCT03040024 Terminated - Otolaryngeal Cancer Clinical Trials

Delirium Prevention With Ketamine in Ear, Nose, and Throat (ENT) Patients

Start date: March 17, 2017
Phase: Phase 4
Study type: Interventional

The goal of this prospective randomized double blinded placebo controlled study is to investigate if a single dose of ketamine in addition to standard anesthesia will reduce the risk of delirium in otolaryngeal cancer patients postoperatively. Ketamine's effect on post-operative pain and opioid use will be measured as well. Electroencephalogram (EEG) will be utilized during the surgical procedure to evaluate its potential as a possible predictive device for delirium.

NCT ID: NCT02903407 Terminated - Critical Illness Clinical Trials

Pain, Agitation and Delirium (PAD) Protocol in the Duke CICU

Start date: September 1, 2017
Phase: Phase 4
Study type: Interventional

This study aims to examine the use of protocol directed sedation using the Duke PAD protocol with the current sedation medications of propofol or dexmedetomidine compared to the PAD protocol with midazolam, per cardiac intensive care unit (CICU) usual care, as an initial step toward understanding the best management of sedation in these patients.

NCT ID: NCT02899156 Terminated - Hypoactive Delirium Clinical Trials

Flumazenil for Hypoactive Delirium Secondary to Benzodiazepine Exposure

FLYP
Start date: March 2016
Phase: Phase 4
Study type: Interventional

Delirium within the intensive care unit (ICU) is associated with poor outcomes such as increased mortality, ICU and hospital length of stay (LOS), and time on mechanical ventilation. Benzodiazepine (BZD) exposure is an independent risk factor for development of delirium. Reversal of hypoactive delirium represents a potential opportunity for reducing duration of delirium and subsequent complications. This is a single-center randomized, double-blind, placebo-controlled study of critically ill adult patients with benzodiazepine-associated hypoactive delirium. The hypothesis is that flumazenil continuous infusion may reverse hypoactive delirium associated with BZD exposure and thereby reduce duration of delirium and ICU LOS.

NCT ID: NCT02818764 Terminated - Delirium Clinical Trials

Delirium, Intraoperative Cerebral Perfusion and EEG Abnormalities After Total Hip Arthroplasty

Start date: June 2016
Phase:
Study type: Observational

The overall objective of this study is to test for perturbations in intraoperative electroencephalogram (EEG) , cerebral blood flow (CBF), cerebral metabolic rate of oxygen consumption (CMRO2), oxygen extraction fraction (OEF), and serum and cerebral spinal fluid biomarkers associated with delirium in high risk population having elective hip arthroplasty at Penn Presbyterian Medical Center (PPMC).

NCT ID: NCT02807467 Terminated - Delirium Clinical Trials

Influence of Dexmedetomidine or Propofol on ICU Delirium

Start date: March 1, 2019
Phase: Phase 4
Study type: Interventional

In this randomized study, the investigators aim to test the hypothesis that the reinstitution of a normal circadian rhythm by continuous infusions of dexmedetomidine compared to propofol between 8pm and 6am after diagnosis of hyperactive or mixed delirium, decreases the duration of delirium. The infusions might have to be repeated several times to achieve resolution of delirium.