Clinical Trials Logo

Sleep Apnea, Obstructive clinical trials

View clinical trials related to Sleep Apnea, Obstructive.

Filter by:

NCT ID: NCT03070756 Recruiting - Clinical trials for Obstructive Sleep Apnea

Extended Evaluation of the Efficacy of a Proactive FOT-based Auto-CPAP Algorithm

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

This study implements an extended (post marked) examination of the efficacy of a proactive auto-CPAP algorithm, which is based on the forced oscillation technique (FOT) in a sample of patients with predominantly obstructive sleep apnea. The auto-CPAP algorithm examined in this study is implemented in the medical devices prisma20A and prismaLAB (Löwenstein Medical Technology).

NCT ID: NCT03066765 Completed - Clinical trials for Obstructive Sleep Apnea

LTR for Treatment of Obstructive Sleep Apnea

Start date: February 25, 2016
Phase: N/A
Study type: Interventional

Study of tongue implant for treatment of obstructive sleep apnea

NCT ID: NCT03066479 Completed - Clinical trials for Obstructive Sleep Apnea

Comparing Fitbit® Quality of Measured Sleep to Sleep Measured by Polysomnography in the Sleep Lab

Start date: August 4, 2015
Phase: N/A
Study type: Interventional

This study is to evaluate a commercial tool on the market (Fitbit®) that also quantifies sleep. No one has studied how pediatric patients perform with it and how accurate it is in measuring their quality of sleep. This study will use the obstructive sleep apnea (OSA) questionnaire completed by parents and Fitbit® together and evaluate how they perform against the polysomnography (PSG).

NCT ID: NCT03066141 Completed - Clinical trials for Coronary Artery Disease

Evaluation of Association Between Obstructive Sleep Apnea and the Severity of Coronary Artery Disease

Start date: February 14, 2017
Phase:
Study type: Observational [Patient Registry]

It is widely accepted that coronary artery disease (CAD) is related to a high mortality. It is predicted that an increase of approximately 21.3 million cardiovascular events and 7.7 million cardiovascular deaths over 2010 to 2030 in China.1 Male sex, diabetes mellitus, hypertension, hypercholesterolemia, obesity and smoking are all traditionally considered as risk factors for CAD. In recent decades, tremendous progress toward the prevention and treatment of traditional cardiovascular risk factors have helped decrease the morbidity and mortality from CAD, but the condition remains a major public health challenge worldwide. Looking into the other potential risk factors (OSA) for CAD, it may help to develop additional preventative strategies and further reduce the incidence and mortality of CAD.

NCT ID: NCT03065322 Completed - Clinical trials for Obstructive Sleep Apnea

The Impact of Obstructive Sleep Apnoea in Women With Polycystic Ovary Syndrome.

Start date: February 13, 2017
Phase:
Study type: Observational

Women with PCOS and OSA, compared to women with PCOS only, have more severe clinical and biochemical features of PCOS and impaired QoL. This is an observational cross-sectional study in a secondary care PCOS clinic in the WISDEM Centre, University Hospital Coventry. The primary aim of this study is to examine the relationship between OSA and impaired QoL in women with PCOS. Study secondary outcomes are to examine the relationship between OSA and the clinical and biochemical features in women with PCOS.

NCT ID: NCT03064204 Completed - Clinical trials for Obstructive Sleep Apnea

The Pathogenesis of OSA in People Living With HIV

Start date: February 9, 2017
Phase:
Study type: Observational

The purpose of this study is to help us understand how HIV and/or Anti-Retroviral Therapy (ART) may predispose individuals to Obstructive Sleep Apnea (OSA). The traditional risk factors for OSA are weight and age. However, people living with HIV on ART seem to have OSA even when they are thin and young. The study involves a detailed physiological sleep study and an MRI of the head and neck to understand the underlying cause of OSA in those with and without HIV.

NCT ID: NCT03063567 Completed - Clinical trials for Obstructive Sleep Apnea of Adult

Investigation of Predictive Indices to Objectively Guide Choice of CPAP Interface

Start date: August 2014
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) is a prevalent disease, and one that is associated with significant negative impact on long-term survival. There is convincing evidence that treatment of OSA can improve outcome in patients with cardiovascular disease, improve blood pressure and blood glucose control, and improve the overall metabolic syndrome. Treatment is usually with continuous positive airway pressure (CPAP). However, many patients face problems with their CPAP interfaces, affecting their compliance and response to treatment. Proper mask fit is important in decreasing air leak and increasing comfort, thus leading to better compliance. Currently, the choice of interfaces depends mainly on the experience of the sleep disorder unit (SDU) technicians. Unsuitable choice of interface not only affects response to treatment but also increases medical costs when interfaces need to be replaced to better fitting ones. It is thus important to develop selection criteria to objectively guide the SDU technicians in choosing the suitable interfaces. The objective of this study is to study the facial profile of patients and look for predictive indices that can be used to objectively guide the choice of appropriate interfaces. Frontal and side profile photographs of patients will be taken and facial measurements will be recorded. Patients will then be given a one monthly trial of each of the 3 interfaces (nasal masks, oronasal masks, nasal cushions) in a randomised order. The patients' subjective perception of each of the interface will be assessed and patients will nominate their preferred interface at the end of the trial. The amount of leak and the hours of adherence for each type of interface will also be analysed. A multinomial logistic regression analysis will then be done to look for facial measurements that will predict the interface that patients will be most satisfied with. Hypothesis That measurement of facial structures and clinical features will be able to predict the best-fit CPAP interface for each patient. Study Objective - To determine anthropometric facial measurements and clinical factors important in achieving a good interface fit for each patient - To derive a prediction rule or equation that will be able to accurately predict which interface a patient should be prescribed

NCT ID: NCT03062748 Enrolling by invitation - Clinical trials for Obstructive Sleep Apnea

Predicting Cardiometabolic Risk in Mild-to-Moderate Obstructive Sleep Apnea: Inflammation vs. Apnea/Hypopnea Index

Start date: March 1, 2017
Phase:
Study type: Observational

The purpose of the study is to compare the relative contribution of systemic inflammation vs. Obstructive Sleep Apnea (OSA) severity (as measured by Apnea Hypopnea Index) in predicting cardiovascular and metabolic aberrations associated with mild-to-moderate obstructive sleep apnea.

NCT ID: NCT03061071 Completed - Clinical trials for Sleep Apnea Syndromes

The POSAtive Study: Study for the Treatment of Positional Obstructive Sleep Apnea

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

This study is a prospective, multi-center, randomized crossover of the NightBalance SPT compared to APAP for the treatment of Positional Obstructive Sleep Apnea (POSA).

NCT ID: NCT03061019 Terminated - Clinical trials for Obstructive Sleep Apnea

Comparison of Two Oral Myofunctional Reeducation Methods for Children With Obstructive Sleep Apnea

PERSIST-B
Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Myofunctional therapy has been shown to be effectively reduce symptoms of paediatric sleep apnea. As the effectiveness of reeducation relies on parental involvement and child's compliance, the investigator's research question was to evaluate two methods of myofunctional therapy (daily oral exercices versus a flexible oral appliance, both in combination with nasal hygiene), compared to nasal hygiene alone (control group).