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CPAP clinical trials

View clinical trials related to CPAP.

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NCT ID: NCT05977296 Recruiting - Dysphagia Clinical Trials

Obstructive Sleep Apnea (OSA), Oral Frailty, Dysphagia, Continuous Positive Airway Pressure (CPAP)

Start date: April 14, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects of the CPAP treatment on oral frailty and dysphagia among OSA patients.

NCT ID: NCT03812653 Recruiting - Stroke Clinical Trials

Sleep for Stroke Management and Recovery Trial

Sleep SMART
Start date: May 9, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether treatment of obstructive sleep apnea (OSA) with positive airway pressure starting shortly after acute ischemic stroke or high risk TIA (1) reduces recurrent stroke, acute coronary syndrome, and all-cause mortality 6 months after the event, and (2) improves stroke outcomes at 3 months in patients who experienced an ischemic stroke.

NCT ID: NCT03644121 Completed - OSA Clinical Trials

Adherence to CPAP in Patients With OSA. Ten Year Follow up

Start date: August 1, 2006
Phase:
Study type: Observational

The management of OSA is aimed to improve symptoms and mitigate reduce other health consequences. Continuous Positive Airway Pressure (CPAP) is the recognized treatment for OSA, able to reverse the pathophysiology of OSA and improving sleep continuity, resulting in improvements in daytime sleepiness and quality of life (QoL). However, low adherence to this treatment reduces the potential to achieve these benefits. The aim of this real life retrospective observational study was to assess the adherence to CPAP at 12 month and 10 years. The investigators evaluated also predicitve factors of adherence.

NCT ID: NCT03523013 Completed - Clinical trials for Obstructive Sleep Apnea

The Outcome of CPAP Titration Under Sleep Endoscopy

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

The outcome of CPAP titration under sleep endoscopy: A randomized controlled crossover trial

NCT ID: NCT03273764 Completed - Clinical trials for Respiratory Distress Syndrome in Premature Infant

Clinical RD (Respiratory Distress) Score for Objective Decision Making for Surfactant Therapy

Start date: January 1, 2015
Phase: N/A
Study type: Observational

To develop a comprehensive ʻClinical RD score' for decision making for administration of Surfactant in respiratory distress syndrome in preterm infants with gestation of 26 0/7 - 34 6/7 weeks and to assess the validity of this ʻclinical RD score' on a different subgroup of patients with similar gestational age.

NCT ID: NCT03121781 Recruiting - Clinical trials for Respiratory Distress Syndrome

Diaphragm Electrical Activity of Preterm Infants on nCPAP With Binasal Prongs Versus RAM Cannula

Start date: November 1, 2016
Phase: N/A
Study type: Interventional

Preterm babies have immature lungs and frequent pauses in their breathing which often necessitates breathing support. Nasal Continuous Positive Airway Pressure (nCPAP) is one of the most commonly used tools, but the standard interfaces (prongs or mask) may cause nasal-septal injury and discomfort. The RAM cannula is another interface that consists in soft and curved prongs to avoid this nasal injury, but as the seal is not 100%, suboptimal delivery of airway distending pressure could result if they are used to deliver CPAP, as compared to standard interfaces. The investigators plan to study very low birth weight preterm babies who are generally well but require some support with their breathing. By inserting a special feeding tube with sensors into the stomach, the investigators can measure the electrical activity of the diaphragm (EAdi), which is an important muscle for breathing. By analyzing EAdi in babies receiving nCPAP either with prongs or ram cannula, the investigators will be able to measure and compare how each method of support affects a baby's breathing. This important study will help us determine the most appropriate breathing support for preterm babies.

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.

NCT ID: NCT00482040 Terminated - Clinical trials for Apnea of Prematurity

Randomized Trial Investigating Four Nasal CPAP Systems in the Management of Apnea of Prematurity

Start date: March 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate four different nasal continuous pressure systems, which are usually applied on our neonatal intensive care unit, with regard of their effect on bradycardia and desaturations in preterm infants.