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Pulmonary Valve Insufficiency clinical trials

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NCT ID: NCT00922857 Completed - Clinical trials for Respiratory Insufficiency

Influence of Muscular Atrophy on Biological and Functional Benefit of Respiratory Rehabilitation in Patients With Chronic Respiratory Failure

INSPIRE
Start date: April 2005
Phase: N/A
Study type: Interventional

The prevalence of chronic respiratory failure (CRF) is increasing worldwide and will become the 3rd cause of death by 2020. At the stage of the disease requiring ventilatory assistance, this relates to 50,000 patients in France, life expectancy is very limited, and quality of life is poor. CRF led to a reduction in muscle mass, which is found in 35 and 55% of patients, in some to a profound cachexia. A reduced fat free mass (FFM) is a factor associated with a poor tolerance to exercise and an halved survival. The exact causes and mechanisms leading to cachexia are not yet established. Recently, a chronic inflammatory condition has been quoted as a putative cause. This chronic inflammation would involve the molecular mechanisms leading to poor regulation of the balance of synthesis / protein degradation in muscle. A decrease in plasma and muscle amino acids was found among patients with a low FFM.. In addition, a decrease of plasma levels of some anabolic hormones, GH and androgens or IGF-1 has been found that could explain a lack of protein synthesis. It is now well established that respiratory rehabilitation, including a program of exercise reconditioning, increases tolerance to exercise and improve the quality of life. Besides the classical type of endurance exercises stimulating the cardio-respiratory system, it is suggested to add resistance exercises. Several studies have reported the benefit of this strategy but the link with intracellular molecular pathways has not been described; moreover, it is unknown whether the existence of an initial muscular atrophy influences the gain in muscle strength/mass.

NCT ID: NCT00885898 Completed - Respiratory Failure Clinical Trials

Out-of-Hospital Non-Invasive Ventilation for Patients With Acute Respiratory Failure

NIV
Start date: March 2005
Phase: N/A
Study type: Interventional

In the past, patients suffering from acute respiratory failure had to be treated with Oxygen and specific medication, or - if this had not been sufficient - had to be anesthesized and had to undergo endotracheal intubation for invasive ventilation. Nowadays, since emergency ventilators are available that can be used for non-invasive ventilation, the purpose of this study is to investigate if non-invasive ventilation is safe, feasible and effective for the treatment of acute respiratory failure and if less patients will need to be intubated out-of-hospital as well as in the further course.

NCT ID: NCT00835809 Completed - Clinical trials for Acute Respiratory Insufficiency

Multi Marker Approach Interest in Emergency in Acute Respiratory Insufficiency Diagnostic

BIO-IRA
Start date: October 2008
Phase: N/A
Study type: Observational

Biomarkers have an interest in clinic diagnostic ,therapeutic and prognosis in pathophysiologic situation including cardiovascular.But interest of biomarkers in diagnostic care of severe acute respiratory insufficiency remains to clear. We propose to determine the more relevant marker combination in this case.

NCT ID: NCT00817804 Completed - Respiratory Failure Clinical Trials

Cross-over Comparison of the V60 System to Other Bi-Level Noninvasive Ventilators

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

The purpose of this study is to compare a new noninvasive ventilator to existing ventilators already used for patient care.

NCT ID: NCT00817297 Completed - Respiratory Failure Clinical Trials

Cross-over Comparison of the V60 System to Other Bi-Level Noninvasive Ventilators

Start date: January 17, 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to compare a new noninvasive ventilator to existing ventilators already used for patient care.

NCT ID: NCT00814099 Completed - Lung Diseases Clinical Trials

Sedation Management in Pediatric Patients With Acute Respiratory Failure (The RESTORE Study)

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

People with acute respiratory failure usually require the use of an artificial breathing machine, known as a mechanical ventilator. Sedative medications, which help keep people calm and reduce anxiety, are often prescribed for children who are on mechanical ventilators. However, the longer that sedative medications are used, the longer a child may need to remain on mechanical ventilation. This study will evaluate the effectiveness of a team approach to sedation management that aims to reduce the number of days that children with acute respiratory failure require mechanical ventilation.

NCT ID: NCT00810498 Completed - Respiratory Failure Clinical Trials

Trilogy Comparison Study - Adults

Start date: March 12, 2008
Phase: N/A
Study type: Interventional

The objective of this study (Part II) will be to compare the performance of the Trilogy device and a conventional ventilator (participant's current device). Both devices will be set to the participants' current mode and prescription settings.

NCT ID: NCT00784004 Completed - Clinical trials for Respiratory Insufficiency

Investigation of Efficiency of Breathing With Different Breathing Patterns

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

Our aim in this study is to investigate the efficiency of the breathing with different breathing patterns. Ten volunteers and twenty patients having respiratory problems will be coached on their breathing through specific masks which will provide four different breathing patterns. These patterns will be 1) Breathing in through the nose only and out through the mouth only 2) Breathing in through the mouth only and out through the nose only 3) Breathing in and out through the nose only 4) Breathing in and out through the mouth only The data obtained from volunteers and patients will be compared within and between the groups.

NCT ID: NCT00741949 Completed - Clinical trials for Respiratory Insufficiency

Broncho-alveolar Lavage Under Noninvasive Ventilation With Propofol TCI in Patient With AHRF

SEDA-FIBRO
Start date: September 2008
Phase: Phase 3
Study type: Interventional

Fiberoptic bronchoscopy (FOB) is an important tool for the diagnosis of pulmonary diseases, more particularly in infectious pneumonia. In patients with severe acute hypoxemic respiratory failure, FOB may be contra-indicated until the patient is intubated and control of its oxygenation obtained. In the literature several authors showed that performing FOB under non invasive ventilation (NIV) preserved oxygenation of the patient; and the recent French Consensus on NIV recommends performing FOB under NIV in patients with acute hypoxemic respiratory failure. Nevertheless this procedure remains uncomfortable in most patients with respiratory failure. In addition, patient's agitation may lead to desaturation, and compromise the realization of FOB.

NCT ID: NCT00722826 Completed - Clinical trials for Pulmonary Regurgitation After Repair of Tetralogy of Fallot

Tetralogy of Fallot Seed Grant

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

Patients with pulmonary regurgitation after surgical correction of ToF over 13 years old will be recruited from the UCSF adult congenital heart disease clinic. Since there is no data in the literature describing the prevalence of abnormal MRI volumetric and functional parameters in asymptomatic patients with PR after ToF repair, a pilot study with 30 patients will be conducted. Increase in sample size may be necessary in the future to accurately interpret the data. After informed consent is obtained, clinical history and physical examination as well as review of old charts will be performed to characterize these patient's clinical status. All patients will undertake a graduated supine bicycle exercise test with MVO2 measurement to assess exercise capacity. MRI studies will be performed in a 1.5 tesla unit. SSFP cine images will be obtained in the short-axis plane encompassing the entire heart. Velocity-encoded cine MR images will be obtained perpendicular to the direction of blood flow in the main pulmonary artery. Volumetric and flow analysis will be performed in a separate dedicated workstation by a radiologist. End-diastolic volume, end-systolic volume, ejection fraction, total ejection fraction and pulmonary regurgitant fraction will be calculated.