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Apnea clinical trials

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NCT ID: NCT03654456 Recruiting - Sepsis Clinical Trials

Impact of Sleep Apnea on Sepsis Mortality

Start date: May 28, 2018
Phase:
Study type: Observational

By clinical record review, this retrospective study aims to compare the mortality of sepsis patients with versus without obstructive sleep apnea, who were diagnosed and treated in Taipei Veterans General Hospital, Taiwan.

NCT ID: NCT03651648 Recruiting - Clinical trials for Apnea of Prematurity

Apnea Treatment in Premature Infants Using an Automatic Vibro-tactile Stimulator Triggered by the Detection of Apnea-bradycardia.

SENSITACT
Start date: October 18, 2019
Phase: N/A
Study type: Interventional

The goal of the SENSITACT system is to activate an adaptive kinesthetic stimulation to treat apnea-bradycardia events on preterm infants, while minimizing deleterious effects, in particular arousals that can be due either to respiratory efforts or to kinesthetic stimulation itself. This novel system will provide an alternative treatment to apnea-bradycardia, with improved patient comfort and autonomy. In particular, it may become a complementary solution for the current treatments (Manual stimulation by caregivers, continuous or intermittent nasal positive pressure ventilation and methylxanthine therapies) that do not appear to be optimal and usually only allow a partial reduction in the number and severity of apneas.

NCT ID: NCT03646552 Recruiting - Clinical trials for Obstructive Sleep Apnea

A Study to Examine the Efficacy of a Therapeutic THX-110 for Obstructive Sleep Apnea

Start date: June 4, 2018
Phase: Phase 2
Study type: Interventional

This is a sponsored proof of concept study with the purpose to examine the safety, tolerability and feasibility of THX-110 (Dronabinol (synthetic Δ9-THC) and PEA) for the treatment of adults with Obstructive Sleep Apnea.

NCT ID: NCT03635918 Recruiting - Sleep Apnea Clinical Trials

Extensive Prospective Validation Study of the NightOwl Home Sleep Apnea Test

Start date: August 15, 2018
Phase: N/A
Study type: Interventional

Extensive Prospective validation study of the NightOwl, a Type IV home sleep apnea test (HSAT), compared to traditional PSG and HSAT monitors.

NCT ID: NCT03621566 Recruiting - Central Sleep Apnea Clinical Trials

Belgian Central Sleep Apnea REgistry

B-CARE
Start date: June 25, 2018
Phase:
Study type: Observational [Patient Registry]

This study evaluates different factors that determine the treatment choice and treatment compliance in patients with central sleep apnea. All patients will receive routine care (registry).

NCT ID: NCT03563118 Recruiting - Clinical trials for Obstructive Sleep-Apnea Syndrome

Evaluation of Prolidase in Obstructive Sleep Apnea Syndrome

Start date: July 1, 2018
Phase:
Study type: Observational

Obstructive sleep apnea (OSA) is a highly prevalent breathing disorder in sleep. We have aimed to evaluate the relationship between OSA and prolidase activity, the oxidative stress index (OSI), total antioxidative capacity (TAC), and total oxidative capacity (TOC) and the relationship between carotid intima media thickness (CIMT).

NCT ID: NCT03547596 Recruiting - Clinical trials for Erectile Dysfunction

Impact of Treatment of Obstructive Sleep Apnea Syndrome by Continuous Positive Airway Pressure Equipment at Night on the Lower Urinary Tract Symptoms and the Erectile Dysfunction

Start date: April 29, 2018
Phase:
Study type: Observational

To treat lower urinary tract symptoms (LUTS) and erectile dysfunction (ED), we mainly have symptomatic drug treatments. Some patients are resistant to the treatments that we have or are forced to stop treatments because of side effects. It would be interesting to focus on comorbidities and to evaluate whether it is possible to improve the urological symptoms by taking care the comorbidities, which would consist in an etiological treatment of the urological symptoms. The aim of the study is to evaluate the evolution of low urinary tract disorders (LUTS) and erectile dysfunction (ED) in patients with obstructive sleep apnea syndrome (OSAS) following by continuous positive airway pressure equipment (CPAP) at night. Participation in the study will be offered to all patients, men and women, consulting or hospitalized in the sleep unit of the department of pneumology CHU of Reims for a nocturnal ventilatory polygraphy or a polysomnography diagnostic of OSAS. Men will complete three questionnaires about LUTS and DE, women one questionnaire about LUTS. The questionnaires will be completed twice, the first time when consulting at the sleep unit for nocturnal ventilatory polygraphy or a polysomnography diagnostic of OSAS ; the second time during the pneumology consultation three months later. We will compare the results between the questionnaires to assess whether OSAS equipment with CPAP has improved urologic symptoms. If the management of OSAS allows an improvement of lower urinary tract disorders and / or an improvement of erectile dysfunction, these results would be interesting for the management of patients resistant to symptomatic drug treatments or to stop them because of iatrogenic side effects. Etiological rather than symptomatic management would also have long-term benefits, both in improving the overall quality of life of the patient and in the medical and economic field. It might be interesting to identify in urology consultation among patients consulting for LUTS or ED, patients at risk of presenting OSAS and referring them to a pulmonologist to manage OSAS if it exists, from the beginning of the urological care.

NCT ID: NCT03526016 Recruiting - Sleep Apnea Clinical Trials

Sleep Apnea in Acromegaly After Surgery

Start date: February 21, 2018
Phase:
Study type: Observational

Sleep apnea is common in acromegaly and both diseases are independently associated with hypertension and insulin resistance contributing to increased morbidity and mortality. Respiratory polygraphy is a simpler alternative to in-laboratory polysomnography for the management of more symptomatic patients with obstructive sleep apnea. The aim of this study is to evaluate the prevalence of sleep apnea by respiratory polygraphy, and to analyze the effect of transsphenoidal surgery on sleep apnea.

NCT ID: NCT03487185 Recruiting - Preeclampsia Clinical Trials

Continuous Positive Airway Pressure (CPAP) for Sleep Apnea in Pregnancy

SLEEP
Start date: August 3, 2018
Phase: N/A
Study type: Interventional

A randomized controlled trial of 1,500 women to assess whether treatment of obstructive sleep apnea with continuous positive airway pressure (CPAP) in pregnancy will result in a reduction in the rate of hypertensive disorders of pregnancy.

NCT ID: NCT03463785 Recruiting - Clinical trials for Obstructive Sleep Apnea of Adult

Does Race Make a Difference in Obstructive Sleep Apnea?

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

Obstructive sleep apnea (OSA) is a sleep-related breathing disorder, often associated with a compromised upper airway space and an increase in upper airway collapsibility. The anatomical and functional abnormalities of the upper airway play an important role in the pathogenesis of OSA. It is hypothesized that there is racial variation in the craniofacial characteristics among OSA patients. However, inter-race comparisons based on previous studies can be problematic due to variation in measurements, OSA definitions and the sample size. Besides, to our best knowledge, there is no studies that made direct inter-race comparisons in the upper airway anatomy. Therefore, studies on inter-race comparisons of the upper airway characteristics are needed to further understand the role of race in the upper airway anatomy of the OSA patients. This would provide more insights into the pathophysiology of OSA, and could result in the development of new effective treatment strategies for OSA patients.