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Sleep Apnea, Obstructive clinical trials

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NCT ID: NCT01715194 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome

Telemedicine to Enhance Adherence to CPAP Therapy in Patients With OSAS

Start date: December 2012
Phase: N/A
Study type: Interventional

We hypothesize that the use of telemedicine combined with support interventions by short messages, telephone calls and ambulatory visits to control CPAP treatment during the first month improves adherence and reduces unresolved side effects of therapy. The primary objective of an OSAS treatment program is to successfully implement indicated CPAP in the highest possible proportion of patients in order to lower the proportion of untreated OSAS in the population. On an individual basis, it has been shown that a longer duration of CPAP use is associated with better outcomes in terms of daytime functioning and in the control of metabolic and blood pressure effects of CPAP. For our study, we have therefore decided to use 2 co-primary endpoints, taking into account both aspects of adherence mentioned. Cardiovascular complications are a major concern in OSAS patients. Effective CPAP treatment has been shown to reduce surrogate measures of cardiovascular risk. We hypothesize that intensified efforts for CPAP adherence with telemedicine has a positive impact on a number of surrogate measures of the cardiovascular risk at 1 and 6 months of treatment.

NCT ID: NCT01703663 Completed - Clinical trials for Obstructive Sleep Apnea

Nasal EPAP for Stroke Patients With Sleep Apnea: a Pilot Trial.

Start date: November 2012
Phase: Phase 2
Study type: Interventional

Specific aim: To test the effects of nasal expiratory positive airway pressure (EPAP) therapy on sleep apnea severity among patients with recent ischemic stroke. Hypothesis 1: Ischemic stroke patients with sleep apnea will have less severe sleep apnea, as measured by the apnea-hypopnea index (AHI), with nasal EPAP therapy compared with a control night. Hypothesis 2: Ischemic stroke patients will have higher mean levels of oxygen saturation with nasal EPAP therapy compared with a control night.

NCT ID: NCT01699139 Completed - Clinical trials for Sleep Apnea, Obstructive

The Effect of Positional Device on the Obstructive Sleep Apnea in Patients With Ischemic Stroke

Start date: August 2012
Phase: N/A
Study type: Interventional

Supine positioning was reported to increase upper airway collapsibility, apnea frequency and duration. Positional therapy, designed to minimize supine sleep, was reported to be beneficial in the general sleep apnea population. As supine sleep is very common in stroke patients, positional therapy might also have therapeutic effects. Given differences between stroke patients with sleep apnea and the general sleep apnea patient, such as rolling ability, body mass index and daytime sleepiness, positional therapy results in the general population may not be applicable to the stroke patient. The effects of positional therapy in ischemic stroke patients with OSA have not been well-investigated. We therefore performed a pilot randomized, controlled, cross-over study to test the following hypotheses: (1) positional therapy reduces the amount of nocturnal supine positioning in patients with subacute ischemic stroke, and (2) severity of sleep apnea improves, as reflected by apnea-hypopnea index (AHI), during positional therapy. The tolerability of positional therapy over a 3-month period in patients with ischemic stroke was also evaluated.

NCT ID: NCT01699126 Completed - Clinical trials for Sleep Apnea, Obstructive

The Endothelium Dysfunction in Patients of Obstructive Sleep Apnea Syndrome

Start date: May 2010
Phase: Phase 4
Study type: Interventional

study Hypothesis: We hypothesize that CPAP could effectively improve the endothelial dysfunction by anti-inflammatory effect in patients of OSA,and compare to the effect of statin.

NCT ID: NCT01697878 Completed - Obesity Clinical Trials

Consequences of Obstructive Sleep Apnea on Respiratory Function Following Weight-loss Surgery

Start date: March 2012
Phase: N/A
Study type: Interventional

The investigators propose to compare two different treatments, continuous positive airway pressure (CPAP) versus breathing of atmospheric pressure, in subjects with obstructive sleep apnea (OSA)recovering from weight loss surgery in the post anesthesia care unit (PACU). WE hypothesize that subjects with OSA will have a higher Apnea-Hypopnea Index (AHI) with desaturation and the investigators expect that post-operative CPAP treatment in the PACU will significantly improve the AHI and therefore improve patient safety in the PACU. The investigators also hypothesize that subjects with OSA have a greater decrease in oxygen saturation in response to opioid administration by patient-controlled opioid analgesia (PCA).

NCT ID: NCT01695980 Completed - Clinical trials for Sleep Apnea, Obstructive

Laryngeal Mask Airway in Pediatric Adenotonsillectomy

LMA
Start date: August 2012
Phase: N/A
Study type: Interventional

The study will compare how often the tubing kinks when a LMA (laryngeal mask airway) with modified retractor is used compared to use of an endotracheal tube (ETT) and non modified retractor is used.

NCT ID: NCT01690429 Completed - Clinical trials for Obstructive Sleep Apnea

Arousal Analysis by Pulse Wave Amplitude in Patients With Obstructive Sleep Apnea

Start date: June 2012
Phase: N/A
Study type: Interventional

Photoplethysmography is an easy non-invasive method to detect the pulse wave amplitude (PWA) from a finger. This can be measured using the Somnocheck micro system. A pulse wave amplitude decrease (PWAD) is considered to be a marker for autonomic activation. Detecting the PWAD is a surrogate marker for waking reactions (arousal) which eventually will contribute to assess sleep disruption and resulting performance deterioration. Arousal and performance deterioration and its possible improvement under continuous positive airway pressure (CPAP) therapy will be determined in this study.

NCT ID: NCT01687855 Completed - Clinical trials for Obstructive Sleep Apnoea

Dynamic Alterations of Tongue in Sleep Apnoea Hypopnea Syndrome During Sleep

Start date: February 2003
Phase: N/A
Study type: Observational

The aim of this study was to evaluate the dynamic changes of the tongue in patients with obstructive sleep apnoea hypopnea syndrome (OSAHS) during sleep and while awake by using Ultrafast Magnetic Resonance Imaging (UMRI)

NCT ID: NCT01676181 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome in Children

ATT Compared With ATE in OSAS Children

RCT ATE/ATT
Start date: November 2011
Phase: N/A
Study type: Interventional

Non-inferiority hypothesis; adenotonsillotomy is equally good as adenotonsillectomy in treating obstructive sleep apnea syndrome (OSAS) in children after one, three and ten years.

NCT ID: NCT01672606 Completed - Clinical trials for Neuromuscular Blockade

Effect of Rocuronium on the Acute Hypoxic Ventilatory Response in Patients With Obstructive Sleep Apnea

Start date: May 2012
Phase: N/A
Study type: Interventional

This study describe the effect of partial neuromuscular blockade of rocuronium on the acute hypoxic ventilatory response in patients with OSA before and after 3 month of CPAP treatment.