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Delirium clinical trials

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NCT ID: NCT02509949 Recruiting - Clinical trials for Postoperative Delirium After Living Donor Renal Transplantation

Effects of Dexmedetomidine on Delirium After Living Donor Renal Transplantation in Adult Patients

Start date: May 2015
Phase: Phase 4
Study type: Interventional

Delirium, an acute change in mental status, is a serious medical complication among hospitalized patients. Syndrome of delirium involves agitation, sleep disturbance, affective disorders and cognitive disruptions. One vulnerable period for developing delirium is in the postoperative days. Postoperative delirium often initiates a cascade of adverse consequences including an increase in length of stay and hospital costs, and greater mortality. The investigators have observed that the incidence of postoperative delirium in patients after renal transplantation is about 20-30% in our hospital. Several studies have revealed that dexmedetomidine, as a widely used sedative during anesthesia, can decrease the incidence of postoperative delirium after cardiac surgery. The investigators aim to examine whether administration of dexmedetomidine can reduce postoperative delirium after living donor renal transplantation in adult patients.

NCT ID: NCT02509221 Completed - Clinical trials for Delirium on Emergence

Effect of Duration of Exposure of Anesthesia With Sevoflurane on Emergence Delirium

Start date: July 2015
Phase:
Study type: Observational

Emergence delirium which is a phenomenon seen commonly in preschool kids anesthetized with Sevoflurane. Restless recovery from anesthesia may not only cause injury to the child or to the surgical site, but may also lead to the accidental removal of surgical dressings, IV catheters, and drains. is one of the The purpose of the study is to find whether duration of exposure to Sevoflurane has any effect on the incidence of Emergence Delirium.

NCT ID: NCT02507609 Completed - Hip Fractures Clinical Trials

Deep Neuromuscular Block on Cytokines Release and Postoperative Delirium

Start date: September 8, 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the relationship between the degree of neuromuscular block, the release of cytokines and clinical outcomes in elderly patients undergoing orthopedic surgery. Investigators hypothesize that deep neuromuscular blockade decreases the release of cytokine and the incidence of postoperative delirium in elderly patients undergoing orthopedic surgery, compared with moderate neuromuscular blockade.

NCT ID: NCT02489734 Completed - Clinical trials for Delirium on Emergence

Post Extubation Delirium and End-tidal Sevoflurane Concentration

Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the incidence of emergence delirium will be reduced when end-tidal concentration of sevoflurane decreases.

NCT ID: NCT02489097 Terminated - Anesthesia Clinical Trials

International Substudy Enigma2 on Postoperative Cognitive Disorders

ISEP
Start date: September 2013
Phase: Phase 4
Study type: Interventional

The study is a substudy of the Enigma2 trial (NCT00430989) which aims at investigating the effectiveness and safety of nitrous oxide (N2O) in anaesthesia.The substudy focus is on postoperative cognitive disorders. Substudy Hypothesis: In patients undergoing anaesthesia for major surgery, administration of N2O will reduce postoperative cognitive disorders when compared with otherwise identically managed surgical patients not receiving N2O as a component of their anaesthesia.

NCT ID: NCT02481115 Completed - Clinical trials for Cognitive Impairment

Validation of the PreSchool Confusion Assessment Method for the Intensive Care Unit (psCAM-ICU)

Start date: February 2013
Phase: N/A
Study type: Observational

The investigators hypothesize that critical care trained registered nurses and physicians can perform measurements of cognitive impairment in critically ill pediatric patients in a reliable and valid manner. To test this hypothesis, the investigators will incorporate an instrument (psCAM-ICU) to assess both components of consciousness, arousal and content, in critically ill pediatric patients at least 6 months to children 5 years of age, both on and off mechanical ventilation, and compare these assessments to those of the reference standard.

NCT ID: NCT02478736 Completed - Clinical trials for Postoperative Delirium After On-pump Cardiac Surgery

Preoperative Transcranial Doppler as a Predictor for Delirium Following On-pump Cardiac Surgery

Start date: June 2015
Phase: N/A
Study type: Observational

Postoperative delirium is an important problem in patients undergoing major cardiac surgery and associated with more complicated hospital course, increased hospital length of stay and total postoperative cost. A study shows that a low preoperative cerebral oximetry (rSO2) is associated with postoperative delirium after on-pump cardiac surgery. Another study showed that patients who underwent cardiac surgery with reduced cerebral blood flow (CBF) velocity in the left middle cerebral artery (MCA) preoperatively are at greater risk for postoperative cognitive dysfunction (POCD). Therefore, the investigators hypothesize that lower perioperative rSO2 and reduced preoperative mean flow velocity (MFV) of MCA are good predictors of the postoperative delirium in the patients undergoing the on-pump cardiac surgery.

NCT ID: NCT02466373 Completed - Critical Illness Clinical Trials

Pharmacokinetics and Clinical Effects of Escalating Doses of Clonidine in ICU Patients

Clokin1
Start date: December 2016
Phase: Phase 3
Study type: Interventional

This study is developed for assessing the pharmacodynamic and pharmacokinetic properties of intravenous (IV) clonidine in critically ill patients on the ICU, and to estimate the optimal dosing strategy for IV clonidine.

NCT ID: NCT02465307 Active, not recruiting - Delirium Clinical Trials

Intelligent Intensive Care Unit

ICU_Delirium
Start date: February 2016
Phase:
Study type: Observational

Delirium, as a common complication of hospitalization, poses significant health problems in hospitalized patients. Though about a third of delirium cases can benefit from intervention, detecting and predicting delirium is still very limited in practice. A common characterization of delirium is change in activity level, causing patients to become hyperactive or hypoactive which is manifested in facial expressions and total body movements. This pilot study is designed to test the feasibility of a delirium detection system using movement data obtained from 3-axis wearable accelerometers and commercially available camera with facial recognition video system in conjunction with electronics medical record (EMR) data to analyze the relation of whole-body movement and facial expressions with delirium.

NCT ID: NCT02433041 Completed - Clinical trials for Postoperative Delirium

Baden Prevention and Reduction of Incidence of Postoperative Delirium Trial

PRIDe
Start date: July 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to find out whether postoperative delirium can be more properly prevented by the combination of determined preventive agents in past studies. Further on the investigators measure pre- and postoperative cortisol, neuron specific enolase (NSE) and S-100beta levels.