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Parasomnias clinical trials

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NCT ID: NCT03332407 Completed - Sleep Disorder Clinical Trials

Does Preoperative Sleep Quality Affect the Postoperative Emergence Delirium in Children Undergoing Strabismus Surgery

Start date: May 2, 2017
Phase: N/A
Study type: Observational

Sleep is important in maintaining the physiological function of the human body. Recently several studies have reported that preoperative sleep quality is associated with postoperative emergence delirium (ED) The ED is a common in pediatric patients undergoing general anesthesia with sevoflurane, but studies on the association of sleep quality have been rare. The investigators, therefore, aimed to investigate the relationship between postoperative delirium and pre and postoperative sleep quality in pediatric patients receiving strabismus surgery through this study

NCT ID: NCT03326765 Recruiting - Sleep Disorder Clinical Trials

Characterizing Sleep Disorders in Children and Adults With Tuberous Sclerosis Complex (TSC)

Start date: September 27, 2017
Phase: N/A
Study type: Interventional

The proposed research project is aimed at further characterization of sleep problems and evaluation of their impact in children and adults with TSC, excluding epilepsy as contributing factor. Questionnaire-based studies have shown that sleep problems occur in up to half of the children and a third of adults with tuberous sclerosis complex (TSC). However, there is only limited information on the nature of sleep problems and their impact on patients with TSC and their families.

NCT ID: NCT03318302 Completed - Sleep Disturbance Clinical Trials

Sleep and Exposure to Screens of Digital Media Devices in Israel

Start date: February 1, 2017
Phase: N/A
Study type: Observational

The aims of this survey are to assess the relationships between exposure to screens of digital media devices, sleep patterns, and daily function such as subjective sleepiness and attention abilities in adult Israel population

NCT ID: NCT03317912 Not yet recruiting - Sleep Disturbance Clinical Trials

Perioperative Lignocaine and Sleep Disturbance

Start date: December 2017
Phase: Phase 4
Study type: Interventional

The aim of this clinical trial is to study the effect of an intravenous infusion of lidocaïne in a multimodal analgesic protocol on the architecture sleep during the first postoperative night.

NCT ID: NCT03307005 Completed - Heart Failure Clinical Trials

Improving Sleep Quality in Heart Failure

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

Poor sleep quality is common in patients with heart failure. The limited available evidence intimates that improving sleep quality in patients with heart failure may improve morbidity and quality of life in this patient population. However, there is a paucity of evidence assessing the use of effective pharmacologic therapies in heart failure. The nonbenzodiazepine, GABA receptor agonist, zolpidem, has been found to have considerable benefits over traditional benzodiazepines as a soporific medication. The investigators hypothesize that zolpidem will safely improve sleep quality in patients with heart failure.

NCT ID: NCT03304938 Completed - Clinical trials for Diabetes Mellitus, Type 2

Lavender Aromatherapy on Sleep Quality and Metabolic Parameters of Type 2 Diabetic Patients With Insomnia

LavenAromDM
Start date: February 1, 2018
Phase: N/A
Study type: Interventional

This study is designed as cross-over double-blind placebo-controlled randomized clinical trial that 40 diabetic patients with sleep disorder with the inclusion criteria will enter into the study and randomly assign to first intervention and first placebo groups.The primary outcomes are change in sleep disorder and metabolic parameters that will be evaluated at the end of the study.

NCT ID: NCT03301727 Completed - Insomnia Clinical Trials

Sleeping for Two: RCT of CBT-Insomnia in Pregnancy

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

Cognitive-behavioural therapy for insomnia (CBT-I) has been shown to be an effective treatment for insomnia in multiple populations, including women during pregnancy and postpartum. Online CBT-I has also been shown to be effective and comparable to in-person CBT-I, and shows promise as an accessible treatment alternative to in-person CBT-I for pregnant women experiencing insomnia. As the harmful consequences of insomnia or sleep disturbances have been well documented during late pregnancy, this randomized-controlled trial will compare the efficacy of both in-person and online CBT-I on pregnant women with insomnia to a wait-list control group.

NCT ID: NCT03299114 Completed - Neuropathic Pain Clinical Trials

WHIRLPOOL FOR OSTEOARHRITIS

Start date: November 1, 2015
Phase: N/A
Study type: Interventional

Both neuropathic and nociceptive mechanisms may contribute to the OA pain experience. Aims: The aim of this study was to determine the efficacy of warm whirlpool on pain, disability, quality of life (QoL) and sleep for patients with neuropathic pain.

NCT ID: NCT03277027 Completed - Quality of Life Clinical Trials

Health Related Lifestyle and Quality of Life in Children With Cerebral Palsy

Start date: May 26, 2017
Phase: N/A
Study type: Interventional

The primary aim of this study is assessing physical activity, the quality of sleep and health related quality of life in children with cerebral palsy, and parenting stress of caregivers of the children with cerebral palsy in Korea.

NCT ID: NCT03274505 Recruiting - Stroke Clinical Trials

Sleep Disorders in Transient Ischemic Attack and Stroke: SOMN'AIC Study

SOMN'AIC
Start date: November 14, 2017
Phase:
Study type: Observational

Sleep disorders in the setting of stroke are numerous, including sleep-related breathing disorders, insomnia, excessive daytime sleepiness and restless legs syndrome. Consequences of theses sleep disturbances include impaired functional outcome and quality of life, anxious and depressive troubles and increased cardio-vascular morbi-mortality. Mechanisms underlying sleep disorders in the setting of stroke are complex and still partly elucidated. They probably involve the consequences of the ischemic lesion and of the handicap, but also of associated vascular risk factors and more generally pre-existent medical history, or they could represent themselves a risk factor for stroke. Transient ischemic attack (TIA) is a particular condition in which risk factors and background of patients are similar to that observed in stroke, without any cerebral lesion and no persistent neurological deficit. The main objective of the SOMN'AIC study is to compare the prevalence of sleep disorders in stroke and in transient ischemic attack (TIA). The study hypothesis is that the prevalence of sleep disorders may be higher in stroke than in TIA patients, reflecting the consequences of the lesion and the associated handicap.