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Psychomotor Agitation clinical trials

View clinical trials related to Psychomotor Agitation.

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NCT ID: NCT02720705 Completed - Agitation Clinical Trials

Transbucal Dexmedetomidine for Prevention of Sevoflurane Emergence Agitation in Pre-school Children

Start date: May 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to evaluate the efficacy of transbucal dexmedetomidine given in preschool children undergoing tonsillectomy operations in the prevention sevoflurane agitation.

NCT ID: NCT02658188 Completed - Clinical trials for Restless Legs Syndrome

Long-term Efficacy and Safety of Gabapentin Enacarbil in Japanese Restless Legs Syndrome Patients

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

The objective of this study is to evaluate the efficacy and safety of ASP8825 (gabapentin enacarbil) for long-term treatment of restless legs syndrome patients.

NCT ID: NCT02651922 Completed - Clinical trials for Nervous Restlessness

Treatment of Patients Suffering From Nervous Restlessness With PASCOFLAIR®

Start date: September 2014
Phase: N/A
Study type: Observational

The study was carried out as a prospective, non-interventional study with the intention of subsequent process cost analyses (PCA) and also considers quality of life, drug misuse, dependence, adverse events and therapy satisfaction.

NCT ID: NCT02642315 Completed - Clinical trials for Restless Legs Syndrome

The Effect of Horizant (Gabapentin Enacarbil) on Augmentation

XP-IIT-0034
Start date: January 2016
Phase: N/A
Study type: Interventional

Restless Legs Syndrome (RLS) is a common neurological disorder. Augmentation is the main complication during long-term DA treatment of RLS. This study aims to examine effect of Horizant (Gabapentin Enacarbil) on Augmentation in RLS patients.

NCT ID: NCT02617056 Recruiting - Dementia Clinical Trials

Objective Assessment of Behavioral Associations of Patients With Dementia

Start date: January 1, 2016
Phase:
Study type: Observational

It is generally acknowledged that patients with dementia are best cared for at home. However, outbursts of various behavioral disturbances, e.g., combativeness, appear in most cases and often necessitate institutionalization. These outbursts are often without apparent warning, which limits preventive interventions. The measurement of the electrical activity of the skin is well-studied as an indicator of stress or agitation. The investigators propose to monitor the electrical activity of skin in patients with dementia in order to determine whether any sign of agitation may occur before the outburst. If skin electrical activity gives sufficient warning, then preventive interventions may be tried. If successful, the ability to predict and prevent outbursts of behavioral disturbances will allow patients to be cared for at home for longer periods. It is the primary aim of this project to determine whether skin electrical activity gives such a warning; possible preventive measures will be the subject of future studies.

NCT ID: NCT02613052 Completed - Clinical trials for Transesophageal Echocardiography Contrast Agents

Agitated Saline, Albumin, or Propofol-albumin Mixture for Enhanced Contrast in TEE Examinations

Start date: January 2016
Phase: N/A
Study type: Interventional

This is a prospective, randomized, controlled study to determine if albumin and propofol or albumin only will provide superior qualitative contrast enhancement during TEE bubble studies compared to agitated saline. Each patient will receive three randomized bubble studies (agitated saline, albumin, and albumin and propofol) using 10 ml of agitated contrast agent. The albumin and propofol mixture will consist of 7 mL of 5% albumin plus 3 mL of propofol (10 mg/mL). Each patient will undergo qualitative review of all 3 bubble studies by 10 different anesthesiologists and/or cardiologists credentialed to read echocardiographic studies at the time of the surgical procedure, and also with retrospective review of the echo video (~200 studies). A bicaval view will be obtained to record a 20 beat loop for each bubble study. Hemodynamic variables prior to injection of contrast agent; and 30 seconds, 1 minute and 2 minutes after injection will be monitored and recorded.

NCT ID: NCT02612948 Completed - Clinical trials for Psychomotor Agitation

Quetiapine for Delirium Prophylaxis in High-risk Critically Ill Patients

Start date: November 2013
Phase: Phase 4
Study type: Interventional

Scheduled, low-dose quetiapine is effective in preventing delirium in high-risk critically ill, trauma/surgical patients. Prophylaxis also reduced ventilator duration and ICU length of stay.

NCT ID: NCT02590744 Recruiting - Anesthesia Clinical Trials

Effects of Preoperative Using of Eye Patches on Prevention of Emergence Agitation After Cataract Surgery

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

This study is a single-center, prospective, randomized, controlled trial. To investigate if preoperative using of eye patch will decrease emergence agitation, and to provide a better method of decreasing emergence agitation to pediatric ophthalmic anesthesiologists.

NCT ID: NCT02559739 Completed - Stroke Clinical Trials

Sleep Deficiency and Stroke Outcome

Start date: July 2015
Phase:
Study type: Observational

Deficient sleep duration and sleep disturbances - such as insomnia, sleep disordered breathing (SDB) and restless legs syndrome (RLS)- are associated with hypertension and cardio-cerebrovascular morbidity and mortality. Several studies suggest that sleep disorders are frequent after stroke and detrimental for stroke outcome. However, more prospective studies in a large unselected sample of stroke survivors are needed to better investigate the short- and long-term consequences of sleep disturbances on mortality and occurrence of new cardio-cerebrovascular events. Also their pathophysiological mechanisms and their influence on stroke recovery should be better understood. Therefore, the aim of this study is to assess the impact of sleep deficiency and sleep fragmentation on the frequency of new cerebro- and cardiovascular events and death after stroke or transient ischemic attacks, and clinical outcome within one and two years after stroke. The working hypotheses are that stroke survivors with sleep deficiency and sleep fragmentation due to insomnia, sleep-disordered breathing or restless leg syndrome will present: (1) higher mortality from all causes and higher frequency of new cardio-/ cerebrovascular events; and (2) a less favorable clinical outcome. Outcomes will be compared between patients with and without sleep deficiency and fragmentation. Since current clinical practice in cerebrovascular patients does not sufficiently consider sleep disorders in patient's management, this study can help to bring attention to a still overlooked medical problem and change the current standard of management of stroke survivors.

NCT ID: NCT02532608 Completed - Healthy Subjects Clinical Trials

Infra-slow Oscillations During Sleep

SleepD-ISO
Start date: October 2015
Phase: N/A
Study type: Interventional

In this study the investigators plan to systematically characterise infra-slow EEG oscillations during sleep, explore their relationship to the microstructure of sleep, and investigate its role in the physiology and pathophysiology of sleep by co-registration of Full band EEG with polysomnography during wake and sleep in healthy subjects, after sleep deprivation, and in patients with restless legs syndrome/periodic leg movements during sleep (RLS/PLMS).