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Sleep Apnea, Obstructive clinical trials

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NCT ID: NCT03280914 Completed - Obesity Clinical Trials

Epidemiology and Intervention of Obstructive Sleep Apnea Based on Community

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

This observational study in a real-world community was designed to perform epidemiological investigation and assess effect of CPAP intervention of obstructive sleep apnea.

NCT ID: NCT03277963 Completed - Obesity Clinical Trials

Perception of Pain During Obstructive Sleep Apnea Syndrome in Obese Patient

Start date: February 4, 2010
Phase: N/A
Study type: Interventional

Obstructive sleep apnea syndrome (SAOS), very commonly associated with obesity, induces major disturbances in sleep architecture. The hypotheses in this work are twofold: on the one hand, the SAOS could generate pain perception disorders in a population already affected by the mechanical weight constraints, generating potentially painful complications, and on the other hand, the improvement of sleep provided by continuous positive airway pressure (PPC) ventilation could "normalize" the pain perception thresholds. It was shown an early rebound effect after treatment on increasing pain threshold in the healthy subject. We want to check it among obese patients with OSA in early and mid-term.

NCT ID: NCT03272763 Completed - Clinical trials for Obstructive Sleep Apnea

A Development Study to Evaluate a Full-Face Mask for the Treatment of Obstructive Sleep Apnea

Start date: October 9, 2017
Phase: N/A
Study type: Interventional

This investigation is designed to evaluate the comfort, ease of use and performance of a trial nasal mask for the treatment of Obstructive Sleep Apnea (OSA) in the home environment.

NCT ID: NCT03268473 Completed - Clinical trials for Obstructive Sleep Apnea

Effect of Non-surgical Periodontal Treatment on Oxidative Stress and Antioxidant Status in OSAS

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

The main objective of this study is to compare the effect of the non-surgical periodontal treatment on serum and saliva oxidative stress parameters in patients with periodontitis and obstructive sleep apnea syndrome (OSAS) and in patients with periodontitis only.

NCT ID: NCT03267927 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome

Management of Obstructive Sleep Apnea (OSA) in Children and Maxillary and Mandibular Development

SAOS
Start date: November 5, 2017
Phase: N/A
Study type: Interventional

Assessment of the association of maxillary expansion using a rapid palatal expansion, use of a mandibular advancement appliance (MGA™) and of a device allowing sleep in a semi-seated position (Yoobreath™) in patients with Obstructive Sleep Apnea (OAS). MGA™ and YooBreath™ constitute the Yookid system™.

NCT ID: NCT03267667 Completed - Clinical trials for Sleep Apnea, Obstructive

Effect of OSA on RV Heamodynamics and Function

Start date: January 1, 2019
Phase:
Study type: Observational

Correlation of severity of obstructive sleep apnea and function of the right ventricle by means of 2D echocardiography and cardiac MRI

NCT ID: NCT03246477 Completed - Clinical trials for Obstructive Sleep Apnea

Long-term Impact of Maxillomandibular Advancement Osteotomy on Sleep Apnea Patients

MIMOSA
Start date: September 2016
Phase:
Study type: Observational

Background Maxillomandibular advancement surgery (MMA) has demonstrated high success rates, improving both the apnea-hypopnea index and associated patient' quality of life (QOL), in patients diagnosed with obstructive sleep apnea syndrome (OSAS). However, clinical relapse has been described in the target population, especially when associated with significant weight gain. Literature reporting the long-term impact of MMA for OSAS is lacking. The surgeons of the Division of Maxillofacial Surgery already started to perform this type of surgery in 1995. Objectives The investigators aim to evaluate the long-term (minimum 15 years post-surgery) biologic and QOL impact of MMA in patients with OSAS. The biologic impact refers to the stability of hard and soft tissues and polysomnographic results. Study design Retrospective study Both pre- en postoperative clinical imaging, polysomnography and quality of life questionnaires will be retrieved from all patients that were surgically treated with an MMA by one surgeon (CDC) between 01/11/1995 and 01/12/1999. Conclusion Short-term data have shown high success rates for MMA in OSAS patients. However, long-term data are lacking. This retrospective study might provide us with more information about the incidence of clinical relapse fifteen to twenty years after surgery.

NCT ID: NCT03243487 Completed - Clinical trials for Obstructive Sleep Apnea of Adult

ThErapy Adherence Management in Veterans

Start date: August 8, 2017
Phase: N/A
Study type: Interventional

The study is a prospective, randomized, controlled trial studying adherence to positive airway pressure therapy in a population referred to the VA system for the treatment of sleep disordered breathing. The primary aim of the study is to determine if, compared to standard care provided at a VA Sleep Center, the deployment of a structured adherence management program and a web-based information program designed for participants beginning positive airway pressure therapy results in a greater portion of participants meeting Centers for Medicare & Medicaid Services (CMS) adherence requirements (use > 4 hours for >= 70% of days) at 90 days.

NCT ID: NCT03242148 Completed - Clinical trials for Obstructive Sleep Apnea

The Evaluation of the Toffee Nasal Pillows Mask for the Treatment of Obstructive Sleep Apnea

Start date: September 16, 2017
Phase: N/A
Study type: Interventional

This investigation is a prospective, non-randomized, non-blinded study. This investigation is designed to evaluate the performance, comfort and ease of use of the F&P Toffee nasal pillows mask amongst obstructive sleep apnea (OSA) patients. Up to 45 OSA patients will be recruited from the Ohio Sleep Medical Institute (OSMI)

NCT ID: NCT03234530 Completed - Clinical trials for Obstructive Sleep Apnea

World Trade Center Kidney-Link

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

This study focuses on the prevalence and identification of kidney disease among participants of the WTC Health Program and the study team are planning to assess kidney disease in a multi-factorial manner. The first aim of this study is to correlate kidney dysfunction with 9/11 exposure, and the study team predicts that exposure to 9/11 is an independent risk factor in kidney disease among the WTC Health Program participants. Secondly, the study team proposes that a well-established WTC-related condition, obstructive sleep apnea (OSA), is independently associated with kidney disease. In addition, the study team believe there is a temporal causative relationship between evidence of kidney disease and the severity of OSA. Finally, the last aim is to further identify and explore potential mechanisms and phenotypes of kidney disease in participants of the WTC Health Programs. Regardless of whether the analyses support or reject these hypotheses, the findings will be of equally great public health importance. Successful completion of the proposed research would address a critical knowledge gap regarding the risk of kidney damage among this group of patients, and would inform future mechanistic studies with the potential to impact prevention.