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Sleep Disorders clinical trials

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NCT ID: NCT00236080 Completed - Clinical trials for Chronic Shift Work Sleep Disorder

Study of the Efficacy and Multiple-Dose Plasma Concentration-Time Profiles of Armodafinil and PROVIGIL

Start date: August 2005
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare the overnight efficacy and plasma concentration-time profiles of armodafinil and PROVIGIL, after multiple doses, in patients with excessive sleepiness associated with chronic Shift Work Sleep Disorder (SWSD).

NCT ID: NCT00228553 Completed - Narcolepsy Clinical Trials

Extension Study of the Safety and Efficacy of Armodafinil in the Treatment of Patients With Excessive Sleepiness

Start date: May 2004
Phase: Phase 3
Study type: Interventional

A 12 Month, Open-Label, Flexible Dosage Extension Study of the Safety and Efficacy of Armodafinil (CEP-10953) in the Treatment of Patients with Excessive Sleepiness Associated with Narcolepsy, Obstructive Sleep Apnea/Hypopnea Syndrome, or Chronic Shift Work Sleep Disorder

NCT ID: NCT00207285 Completed - Clinical trials for Sleep Apnea, Obstructive

Sleep Disorders Management, Health and Safety in Police

Start date: May 2005
Phase: N/A
Study type: Interventional

The purpose of the study is to test the effect of a sleep disorders detection and treatment program for police officers on their safety, quality of life, and job performance. The program is called Operation Healthy Sleep. We will develop and test a sleep health detection and treatment program that we aim to apply nationwide to reduce police officer fatigue and stress; enhance the ability of officers and their families to cope with police work; improve the health, safety and performance of law enforcement officers; and thereby improve public safety. Part of this program will include a questionnaire asking about about work hours and health related issues. We will then look at how these survey data relate with data on police officer safety and job performance that we are collecting through police department's databases. Sleep disorders are common and treatable, but often remain undiagnosed and untreated. Police officers work some of the most demanding schedules known, which increases their risk of sleep disorders. The public expects officers to perform flawlessly, but unrecognized sleep disorders lead to severe disruption of sleep, which significantly reduces an individual's ability to think clearly and perform well. In addition, sleep loss and sleep disruption affect personal health, increasing the risk of gastrointestinal and cardiovascular. We also know that sleep loss increases the risk of injury due to motor vehicle crashes. The goals of Operation Healthy Sleep are to improve officers' health, safety, and performance by reducing the impact of fatigue. The study will take place over two years. In the first year, half of the police officers will take part in Operation Healthy Sleep, and in the second year, the second half will participate. We will carefully select the year 1 and year 2 groups so that the data collected across the two years can be validly compared.

NCT ID: NCT00203840 Completed - Sleep Disorders Clinical Trials

Pediatric Sleep Questionnaire: Normalization and Validation Study

Start date: August 2004
Phase: N/A
Study type: Observational

The information gathered from normal pediatric patients seen at the Pediatric Neurology Clinic in the DCAM and LaRabida Children's Hospital will be used to standardize and validate the information gathered from pediatric patients with sleep disorders. This will serve as the information source for a pediatric sleep database.

NCT ID: NCT00203827 Completed - Sleep Disorders Clinical Trials

Pediatric Sleep Questionnaire: Use for Collection of Clinical Data

Start date: September 2004
Phase: N/A
Study type: Observational

The purpose of this study is to develop a questionnaire that can be used for standardized patient information gathering in the clinical setting. This will serve as the information source for a pediatric sleep database.

NCT ID: NCT00195520 Completed - Hot Flashes Clinical Trials

Study Evaluating Totelle® in Menopausal Symptoms and Sexual Function

Start date: December 2004
Phase: Phase 4
Study type: Interventional

To evaluate the tolerability, bleeding patterns and acceptability of Totelle® 1mg administered to a population of Brazilian women in a continuous combined regime for hormone replacement therapy.

NCT ID: NCT00178568 Completed - Sleep Disorders Clinical Trials

Reducing Caregiver Stress and Sleep Disturbances in Patients With Progressive Dementia

Start date: February 2003
Phase: Phase 1
Study type: Observational

People under stress, such as those caring for an ill family member, often have trouble with their sleep. The aim of this study is to see if reducing stress and changing a caregiver's sleep and wake patterns will improve his/her sleep. The investigators also will see whether improvements in sleep result in improved mood, health, and general functioning.

NCT ID: NCT00174174 Completed - Sleep Disorders Clinical Trials

Provigil (Modafinil) Study by Taiwan Biotech Co.

Start date: September 2003
Phase: N/A
Study type: Interventional

The primary objective is to evaluate the therapeutic effect of excessive daytime sleepiness associated with narcolepsy. Both of the subjective and objective sleepiness of the patients were assessed in the experiment by repeat measures.

NCT ID: NCT00172471 Completed - Hemodialysis Clinical Trials

The Relationship Between Sleep Disorders and Cytokine Levels Among Hemodialysis and Peritoneal Dialysis Patients

Start date: n/a
Phase: N/A
Study type: Observational

Sleep disorders are common in patients with end-stage renal disease on both hemodialysis and peritoneal dialysis and are associated with significant medical, psychological and social disturbances. Numerous factors have been suggested as contributing to or associated with the high prevalence of sleep disturbance in this population. Increasing evidence suggests that cytokines are involved in the regulation of sleep and wakefulness and that the communication between the sleep and the immune system is bi-directional. Blood-dialyzer or peritoneum-dialysate interaction during dialysis therapy has the potential to activate mononuclear cells leading to production of inflammatory cytokines. These cytokines are believed to play a significant role in dialysis-associated morbidity and mortality. Nevertheless, a cytokine overproduction may alter sleep pattern in chronic dialyzed patients, thus explaining the presence of sleep disorders in these patients. In the other way, sleep loss may have effects on immune process and secretion of cytokines in chronic dialyzed patients. The purpose of this study was to examine the relationship between quality of sleep and serum cytokine levels in hemodialysis and peritoneal dialysis patients.

NCT ID: NCT00163670 Completed - Sleep Disorders Clinical Trials

The Impact of Sleep Disorders on Motor Vehicle Accidents

Start date: September 2005
Phase: N/A
Study type: Observational

Patients who have sleep disorders may be involved in accidents more frequently than those without. In addition patients who have sleep disorders may have more serious accidents and have increased length of stay.We aim to recruit drivers admitted as a result of a motor vehicle accidents and to ascertain the prevalence of sleep disorders in this group.