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Apnea clinical trials

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NCT ID: NCT00380458 Withdrawn - Clinical trials for Sleep Apnea, Obstructive

Study to Evaluate Recovery From Postoperative Pain After Sleep Apnea Surgery

Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess whether tonsillectomy and UPPP performed using the study device to treat Obstructive Sleep Apnea (OSA) symptoms in adults is associated with less postoperative pain during the 21-day postoperative recovery period compared to electrocautery dissection.

NCT ID: NCT00371293 Active, not recruiting - Inflammation Clinical Trials

The Effects of Obesity and Obstructive Sleep Apnea on Inflammation and Heart Disease

Start date: September 2006
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) is a serious sleep disorder in which a person's breathing is restricted during sleep. Obese individuals with OSA are at an increased risk of inflammation and heart conditions, but it is unknown whether this risk is related to the effects of OSA or obesity. This study will evaluate whether OSA or obesity plays the primary role in inflammation related to heart disease. The study will also determine the independent effects of OSA and obesity on insulin resistance and blood vessel function.

NCT ID: NCT00369759 Completed - Pneumonia Clinical Trials

An Epidemiological Study to Evaluate the RSV-Associated Lower Respiratory Track in Infections in Infants

Start date: September 2006
Phase: N/A
Study type: Observational

The primary objective of this study is to describe the incidence of RSV-associated LRI among infants <1 year of age presenting to the ED during selected shoulder months.

NCT ID: NCT00369005 Completed - Anemia Clinical Trials

Liberal Versus Restrictive Transfusion Guidelines for Preterm Infants

Start date: December 1992
Phase: N/A
Study type: Interventional

The purpose of this study was to determine whether restrictive guidelines for red blood cell (RBC) transfusions for preterm infants can reduce the number of transfusions without adverse consequences.

NCT ID: NCT00317083 Completed - Clinical trials for Sleep Apnea Syndrome

Cough Reflex and Obstructive Sleep Apnea Syndrome

Start date: November 2001
Phase: N/A
Study type: Interventional

Up to 70% of obese patients undergoing bariatric surgery have obstructive sleep apnea syndrome (OSAS). OSAS is responsible for laryngeal sensory impairment. As the afferent neural pathway involved in the initiation of cough is located in the laryngeal epithelium, cough reflex sensitivity may be decreased in obese OSAS patients. The researchers therefore conducted this study to determine the effect of OSAS associated with obesity on cough reflex sensitivity, assessed by cough reflex threshold to an inhaled irritant (citric acid).

NCT ID: NCT00313092 Terminated - Glaucoma Clinical Trials

Obstructive Sleep Apnea Syndrome in Glaucoma

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

The aim of the study is to determine if plasma matrix-metalloproteinase activity can predict glaucoma in patients with OSAS and if the level of plasma matrix-metalloproteinase activity will decrease after one month of nCPAP-treatment.

NCT ID: NCT00310323 Completed - Sleep Apnea Clinical Trials

Hepatic Drug Biotransformation in Children With Obstructive Sleep Apnea

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

The purpose of this research study is to determine the effect of chronic nighttime low oxygen saturations on selected body systems (liver) that break down drugs in children with obstructive sleep apnea syndrome (OSAS).

NCT ID: NCT00310310 Completed - Clinical trials for Sleep Apnea Syndromes

Effect of Self-Management on Improving Sleep Apnea Outcomes

Start date: April 2006
Phase: Phase 2/Phase 3
Study type: Interventional

Obstructive sleep apnea syndrome (OSA) is a common sleep disorder that is associated with serious medical and psychological complications. Nasal continuous positive airway pressure (CPAP) is the treatment of choice for this condition because it is highly effective in reducing the frequency of nocturnal respiratory events, improving sleep architecture, decreasing daytime sleepiness and improving blood pressure. Incomplete patient adherence, however, limits the effectiveness of CPAP therapy and results in sub-optimal patient outcomes. Previous efforts to enhance CPAP adherence have resulted in only modest improvements, have generally not been theory-driven, and have had minimal effects on key patient outcomes such as reduction in OSA symptoms or increase in health-related quality of life (HRQOL). The planned intervention in this proposal, the Sleep Apnea Self-Management Program (SASMP), is based on the rationale that sleep apnea is a chronic disease that requires significant self-care on the part of the patient. We draw on the extensive chronic disease self-management literature to provide a solid theoretical justification for this pragmatic intervention both to better manage key aspects of OSA and to increase CPAP adherence. Chronic disease management programs help reduce symptoms, improve HRQOL, improve treatment adherence, and decrease medical utilization.

NCT ID: NCT00307957 Completed - Clinical trials for Obstructive Sleep Apnea

Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstructive Sleep Apnea

Start date: October 2005
Phase: Phase 4
Study type: Interventional

The Pillar palatal implant procedure is a minimally invasive and commercially available treatment for mild to moderate obstructive sleep apnea (OSA) in the United States and Europe. The implants are placed into the soft area in the roof of the mouth providing support to the soft palate. This research is being done to compare daytime sleepiness and sleep related quality of life after palatal implants.

NCT ID: NCT00305032 Completed - Clinical trials for Obstructive Sleep Apnea

Effect of Endoscopic Gastric Balloon Insertion on Obstructive Sleep Apnea in Patients With Morbid Obesity

Start date: March 2006
Phase: N/A
Study type: Interventional

To investigate the effect of weight loss by gastric balloon insertion on parameters of obstructive sleep apnea.