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Hypoventilation clinical trials

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NCT ID: NCT03449641 Completed - Clinical trials for Obesity Hypoventilation Syndrome

PAP Therapy in Patients With Obesity Hypoventilation Syndrome

Start date: June 1, 2009
Phase: N/A
Study type: Interventional

The role of different levels of compliance and long-term effects of positive airway pressure (PAP) therapy on gas exchange, sleepiness, quality of life, depression and death rate in patients with obesity hypoventilation syndrome (OHS).

NCT ID: NCT03430206 Completed - Clinical trials for Anesthesia; Adverse Effect

Transnasal Humidified Rapid-Insufflation Ventilatory Exchange (THRIVE) Use in Pediatric Procedures

Start date: February 21, 2018
Phase: N/A
Study type: Interventional

THRIVE (Transnasal Humidified Rapid-Insufflation Ventilatory Exchange) refers to the use of high-flow nasal cannula to augment the ability to oxygenate and ventilate a patient under general anesthesia. The use of high-flow nasal cannula oxygen supplementation during anesthesia for surgical procedures has been a recent development in the adult population, with limited data analyzing the pediatric population. This study will determine whether high flow nasal cannula oxygen supplementation during surgical or endoscopic procedures can safely prevent desaturation events in children under anesthesia.

NCT ID: NCT03085537 Completed - Clinical trials for Neuromuscular Diseases

Effectiveness Monitoring of Home Non-invasive Mechanical Ventilation by Digital Diagnosis Platform

PRE-HVNI
Start date: October 1, 2016
Phase:
Study type: Observational [Patient Registry]

The main objective will be to determine the effectiveness of home non-invasive ventilation by flow-time and time-pressure curves analysis in a cohort of patients with this treatment by digital diagnosis platform.

NCT ID: NCT03053011 Completed - Healthy Volunteers Clinical Trials

Evaluation of the Awakening Capability by a Vibrating Bracelet (BRASSARD)

BRASSARD
Start date: February 13, 2017
Phase: N/A
Study type: Interventional

As part of developing a relay alarm project, the aim of the study is to test a sleeper's capability to wake up via a vibrating alarm around the wrist (vibrating bracelet).

NCT ID: NCT02934581 Completed - Clinical trials for Obesity Hypoventilation Syndrome

Prevalence Rate, and Clinical Characteristics of Obesity Hypoventilation Syndrome Via Screening Patients Admitted to Medical Intensive Care Units

Start date: October 29, 2014
Phase:
Study type: Observational

A prospective observation study to screen adult obese (BMI ≥30 kg/m2) patients who were newly admitted to the medical intensive care units and turned out to be diagnosed as Obesity hypoventilation syndrome(OHS). The investigators purpose is to look into the prevalence, predictive factors, and outcomes of OHS in these critically ill patients.

NCT ID: NCT02848118 Completed - Hypoventilation Clinical Trials

Capnography Monitoring in the Bronchoscopic Sedation

Start date: January 2015
Phase: N/A
Study type: Interventional

Procedure sedation of flexible bronchoscopy (FB) comforts patients undergoing FB. Hypoventilation during FB is a concern. The investigators investigate the feasibility of monitoring capnography in FB sedation.

NCT ID: NCT02743624 Completed - Clinical trials for Acute Mechanical Ventilatory Failure

Criteria Analysis for Ventilatory Support Adjustment of Mechanical Ventilation

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

The indications for mechanical ventilation (MV) include excessive work of breathing, with or without evidence of respiratory muscle fatigue. The setting of the MV is still a challenge because it is based on criteria understudied, often subjective and observer-dependent. Despite several studies, to our knowledge has never been done before is the precise definition of the optimal range of ventilatory support. Novel and recognizable diagnostic techniques will be applied. No single parameter of the breathing pattern has good accuracy for the adjustment of ventilatory support. Non-invasive measures such as P0.1 and rate of muscle relaxation may have good accuracy for the adjustment of ventilatory support.

NCT ID: NCT02554110 Completed - Hypoxemia Clinical Trials

Peripheral Nerve Stimulation to Reduce Hypoxic Events

Start date: October 12, 2015
Phase: N/A
Study type: Interventional

This study is designed to determine if using peripheral nerve stimulation in conjunction with pulse oximetry as an adjunct to traditional monitoring in the PACU reduces the frequency and severity of sedation related apnea and hypoxic events.

NCT ID: NCT02551406 Completed - Clinical trials for Neuromuscular Disease

Prognostic Value of Residual Hypoventilation in Mechanically Ventilated Neuromuscular Patients

TcCO2-VAD
Start date: September 2015
Phase: N/A
Study type: Observational

Different tools may be used to monitor the efficacy of home mechanical ventilation. Investigators aimed to compare the prognostic value of the different data obtained by capno-oxymetry in a mechanical ventilated neuromuscular disease's population.

NCT ID: NCT02450071 Completed - Clinical trials for Traumatic Brain Injury

Pre-Hospital Advanced Airway Management in the Nordic Countries

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

Pre-Hospital Advanced Airway Management (PHAAM) is a potentially lifesaving intervention. A recent Danish multicentre single country study demonstrated a 99,7% incidence of successful anaesthesiologist pre-hospital endotracheal intubation, with a PHAAM-related complication rate of 7.9%. A London study revealed a significantly higher intubation failure rate among non-anaesthesiologist physicians. In Scandinavia different types of emergency medical services (EMS) and professions provide PHAAM. The success rate of prehospital endotracheal intubation (PHETI), incidence of difficult intubation and complications in the Nordic countries is not known. The aim of this study is to define PHAAM success rate and complications in different types of Nordic EMS organisations and physician critical care teams. The study is a prospective observational study with collection of PHAAM data according to the template by Sollid et al. in the 12 participating Nordic Countries EMS/HEMS centres and physician critical care teams. The primary endpoint is PHETI success on ≤2 attempts and no complications.