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Psychomotor Agitation clinical trials

View clinical trials related to Psychomotor Agitation.

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NCT ID: NCT02757495 Completed - Clinical trials for Delayed Emergence From Anesthesia

Can Caudal Dexmedetomidine Prevents Sevoflurane Induced Emergence Agitation in Children

Start date: April 2016
Phase: Phase 4
Study type: Interventional

Emergence agitation (EA) is common phenomenon in pediatric patients undergoing general anesthesia by inhalation agents. The incidence of EA was reported to range from 18% to 80%. Sevoflurane now is the inhalational anesthetic agent of choice for pediatrics, Different strategies have been suggested to decrease the incidence and severity of EA. No gold standard technique for treating EA after sevoflurane anesthesia is currently available. The main question is can caudal dexmedetomidine be used for this purpose?

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: 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: 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).

NCT ID: NCT02526277 Completed - Clinical trials for Restless Legs Syndrome

A Study on the Use of the MMF07 Foot Massager and Heat Therapy Treatments for Restless Leg Syndrome

Start date: January 6, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether the MMF07 Foot Massager and/ or heat therapy may improve symptoms of restless legs syndrome (RLS). It will also assess the effect of the MMF07 Foot Massager and/ or heat on quality of life and sleep in people affected by RLS. Participants will be randomly assigned to one of four treatment groups; 1. MMF07 Foot Massager device 2. Heat therapy 3. Heat therapy and the MMF07 Foot Massage device 4. Neither heat nor MMF07 Foot Massager device (no treatment group)