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Parasomnias clinical trials

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NCT ID: NCT00902330 Completed - Breast Cancer Clinical Trials

Cranial Stimulation for Chemotherapy Symptoms in Breast Cancer

Start date: April 2009
Phase: Phase 3
Study type: Interventional

RATIONALE: Cranial microcurrent electrical stimulation (CES) is mild electrical current received through electrodes placed on the earlobes. CES may lessen symptoms in women with breast cancer receiving chemotherapy. It is not yet known whether CES is more effective than sham therapy in reducing symptoms caused by chemotherapy in women with breast cancer. PURPOSE: This randomized phase III trial is studying mild electrical stimulation to see how well it works compared with sham therapy in reducing symptoms caused by chemotherapy in women with stage I, stage II, or stage IIIA breast cancer receiving chemotherapy.

NCT ID: NCT00900159 Completed - Clinical trials for Shift-Work Sleep Disorder

Effects of Daytime Eszopiclone Administration in Shift Workers

Start date: May 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to test the effects of eszopiclone on daytime sleep and overnight wakefulness in shift workers.

NCT ID: NCT00895375 Completed - Psoriasis Clinical Trials

Prevalence of Sleep Disturbances in Psoriasis

Start date: October 2009
Phase:
Study type: Observational

The purpose of this study is to compare the sleep quality of patients with psoriasis to patients without psoriasis.

NCT ID: NCT00878553 Completed - Sleep Disorder Clinical Trials

Study of Sleep-maintenance Activity of 3 Doses of SKP-1041

Start date: May 2010
Phase: Phase 2
Study type: Interventional

SKP-1041 is a new formulation of a marketed sleeping agent called zaleplon. Zaleplon is currently available as Sonata as well as several generic formulations. Sonata and its generics induce sleep soon after ingestion. SKP-1041, however, is a formulation that is designed to become active 2-3 hours after ingestion. It is intended for use in people who have no trouble falling to sleep but who often awaken in the middle of the night. This trial will determine the best dose to prevent those awakenings.

NCT ID: NCT00877162 Completed - Sleep Problems Clinical Trials

The Rocky Sleep Study

Start date: June 2009
Phase: N/A
Study type: Interventional

Night waking with crying can be a distressing and difficult experience for infants and their parents. The investigators want to reduce infant night waking and crying and improve parents' views of their infants' sleep. This study will help the investigators determine whether parents who receive group teaching about infant sleep and follow-up phone calls provided by Public Health Nurses will reduce numbers of infants' night wakes and parents' perceptions of infant sleep difficulties compared with parents who receive a group teaching about infant safety and follow-up phone calls provided by Public Health Nurses. Results from this study will help the investigators improve their practice when assisting parents and infants with sleep problems.

NCT ID: NCT00843843 Completed - Sleep Disorders Clinical Trials

Sleep Length and Circadian Regulation in Humans

HAM
Start date: March 2008
Phase: N/A
Study type: Interventional

This research will examine why sleep restriction reduces the body clock's response to bright light. The results will enable the optimization of the bright light treatment of people who suffer from circadian rhythm sleep disorders, which include shift work sleep disorder, jet lag, delayed sleep phase syndrome and winter depression, thereby improving public health and safety, well-being, mood, mental function, and quality of life.

NCT ID: NCT00831298 Completed - Alzheimer Disease Clinical Trials

Assessment of Sleep Disturbance in Alzheimer Disease

Start date: July 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to study circadian rhythms, or daily cycles of sleep, wake, and activity. The investigators hope to learn how disturbed sleep in Alzheimer's Disease relates to changes in activity cycles, and how sleep disturbances may affect your daytime alertness. This project selects patients suffering from memory problems, or voluntary to be in our Control Group. There are three parts to this study: Sleep Diaries, Behavioral Questionnaire, and Activity Recordings

NCT ID: NCT00830115 Completed - Clinical trials for Gastroesophageal Reflux Disease

Pantoprazole 20/40 mg in the Treatment of Symptomatic Reflux Disease With Focus on Sleep Disorders

PANDA
Start date: January 2009
Phase: N/A
Study type: Observational

The aim of the study was to evaluate the effect of pantoprazole on sleep disorders in patients with NERD (non-erosive reflux disease) or eGERD (erosive gastroesophageal reflux disease). The prevalence and intensity of the sleep disorders were evaluated by a standardized questionnaire. The study was expected to provide further data on safety and tolerability of pantoprazole.

NCT ID: NCT00817674 Completed - Clinical trials for Chronic Kidney Disease

Sleep Disturbances as a Non-traditional Risk Factor in CKD-Actigraphy

CRIC
Start date: November 2007
Phase: N/A
Study type: Observational

To test if usual at home night time sleep duration as measured with activity monitors and questionnaires will predict changes in kidney function as measured by kidney filtration rate and of cardiovascular function as measured by C-reactive protein in the blood. The study will explore the role of decreased sleep time or decreased sleep quality as a non-traditional risk factor for the progression of CKD and for the development of cardiovascular disease in CKD.

NCT ID: NCT00817492 Completed - Clinical trials for Chronic Kidney Disease

Sleep Disturbances as a Non-Traditional Risk Factor in Chronic Kidney Disease- University of Illinois

CRIC
Start date: July 2006
Phase: N/A
Study type: Observational

This study will help determine the relationship between impaired sleep and chronic kidney disease, specifically to determine if sleep disturbances are a risk factor for worsening kidney function.