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Respiration Disorders clinical trials

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NCT ID: NCT01113255 Completed - Clinical trials for Respiratory Diseases

Validation of a Simulated Clinical Evaluation of Ventilators

SIMULVENTI
Start date: March 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the ability of a device reproducing patients' respiratory characteristics to select in-VITRO the most appropriate ventilator for a given pathology.

NCT ID: NCT01047852 Completed - Respiratory Failure Clinical Trials

Noninvasive Ventilation After Extubation in Hypercapnic Patients

VHYPER
Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the efficacy of noninvasive ventilation (NIV) in the prevention of extubation failure and mortality in patients with either chronic respiratory disorders or hypercapnic respiratory failure during spontaneous breathing.

NCT ID: NCT00988000 Completed - Clinical trials for Respiratory Diseases

Initial Specialist Telephone Consultation With New Patients in Secondary Care

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

Consultations with patients by hospital consultants are organised today in a manner which is barely dissimilar from that offered 30 or 40 years ago. Whilst some attempts to improve this process, such as Choose and Book, shorter waiting times and patients' receiving a copy of the correspondence sent to their general practitioner (GP) have improved the situation, there has been little radical change and little thought given to the patient experience. The investigators wish to investigate whether patients' experience of attending respiratory outpatient clinics can be improved by a pre-clinic telephone call with a specialist thereby reducing the number of attendances at the hospital for appointments and investigations and improving overall patient satisfaction.

NCT ID: NCT00864084 Completed - Lung Diseases Clinical Trials

Does Pulmonary Rehabilitation Improve Balance in People With Respiratory Disease?

Start date: April 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether participation in pulmonary rehabilitation improves balance in people with respiratory disease.

NCT ID: NCT00844935 Withdrawn - Clinical trials for Cardiovascular Abnormalities

Electrocardiographic Autonomic Function Measures in Mechanically Ventilated Patients

Start date: September 2011
Phase: N/A
Study type: Observational

This research proposal has two main objectives. The first is to increase understanding of the underlying physiological interactions that occur between the cardiovascular, pulmonary, and ANS during transition between positive pressure mechanical ventilation (MV) and spontaneous breathing. The second is to determine if heart rate variability, (HRV) a reflection of autonomic nervous system (ANS) activity, and autonomic information flow (AIF), a set of nonlinear measures derived from HRV, both measured in the intensive care unit (ICU) can predict patient outcomes including successful weaning and in-hospital recovery time after an episode of cardiopulmonary compromise requiring MV. Hypothesis 1. Transitions between mechanically supported ventilation and spontaneous breathing will disturb cardiovascular synchrony, altering the relationship of HRV, AIF, respiratory rate, and blood pressure; Hypothesis 2. More normal HRV and AIF values, measured during baseline MV and sedation awakening (a period immediately prior to SBT when sedative medications are discontinued) will be associated with easier weaning, and shorter intensive care unit (ICU) and hospital lengths of stay; more abnormal measurements will be associated with longer lengths of stay; Hypothesis 3. AIF is a more sensitive predictor of successful weaning from MV than HRV.

NCT ID: NCT00840723 Completed - Clinical trials for Respiratory Diseases

Bronchoscopy Assisted Sampling of Cells and Fluid From the Lower Respiratory Tract of Human Subjects

SCCOR Bronch
Start date: February 2009
Phase: N/A
Study type: Observational

The purpose of this research study is to collect cells and liquid from the air passages of healthy adults, both smokers and non-smokers. These samples will be used for test-tube studies to explore mechanisms of diseases of the respiratory tract, and to compare the samples between people who smoke cigarettes and people who don't. Obtaining these samples requires an invasive procedure called "bronchoscopy".

NCT ID: NCT00835003 Completed - Clinical trials for Respiratory Disorders

Timing of Planned Caesarean Section and Morbidity of the Newborn

Start date: March 2009
Phase: N/A
Study type: Interventional

The caesarean section rate is rising globally. About 10% of the newborns are submitted to a neonatal department after planned caesarean section, primarily with respiratory disorders. More children are submitted if caesarean is performed earlier in pregnancy. Study hypothesis: More newborns are admitted after planned caesarean at 38 weeks and 3 days of gestation than after 39 weeks and 3 days of gestation. Aim of study: To compare elective caesarean section performed at 38 weeks and 3 days of gestation with 39 weeks and 3 days of gestation. According to this timing to determine the proportion of newborns admitted within 48 hours after birth.

NCT ID: NCT00823056 Completed - Diarrhoea Clinical Trials

The Effect of Probiotics on Infections in Toddlers

Start date: January 2009
Phase: Phase 3
Study type: Interventional

Probiotics has been known as a dietary supplement for a long period. Recent clinical trials indicate that probiotics might have an effect in preventing common infection diseases in children. The investigators hypothesis is: if young children in the age of 6 month to 15 mdr. has a daily intake of a suspension containing probiotics in a period of 9 months, the incidence of diarrhoea and respiratory diseases can be reduced.

NCT ID: NCT00810186 Completed - Apnea Clinical Trials

Continuous Monitoring of Lung Ventilation

Start date: April 2009
Phase: N/A
Study type: Observational

Background: Patients that suffer from respiratory failure and need mechanical ventilation are at risk of further deterioration due to complications induced by progression of lung disease or the mechanical ventilation. The complications usually develop in a progressive manner, but are currently detected relatively late, when there is already severe and life threatening deterioration in patient oxygenation and sometimes irreversible damages. Objective:To measure chest wall dynamics, derived from sensors placed on the chest and abdomen. Methods: The system comprises of patches attached to the chest wall and upper abdomen that include mechanical sensors that measure the mechanics of lung inflation and deflation.

NCT ID: NCT00750074 Completed - Clinical trials for Respiration Disorders

Slope of the Pressure-Time Waveform Predicts Resistance and Compliance in Mechanically Ventilated Subjects

Start date: November 2007
Phase: N/A
Study type: Observational

There are two fundamentally different ways to ventilate critically ill patients: constant flow, volume-preset modes (such as volume assist-control) and pressure-preset modes (such as pressure-control and pressure-support). Critically ill patients suffer mechanical derangements of the respiratory system that raise the work of breathing. Knowledge of these mechanical properties is useful diagnostically and as a measure of response to treatment over time. It has been proposed that only constant flow, volume-preset modes are able to offer diagnostic information about the changes in the subject's lungs in terms of resistance and elastance properties. This study proposes to examine if similar information can be extracted from pressure-preset modes by comparing information from both modes of ventilation.