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Respiratory 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NCT ID: NCT00922532 Withdrawn - Clinical trials for Hypoxic Respiratory Failure With Pulmonary Hypertension

Inhaled Nitric Oxide (INO) In Hypoxic Respiratory Failure

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

This Phase 3, Double-blind, Randomized, Placebo controlled, multicenter study is to confirm the efficacy of inhaled nitric oxide for the management of hypoxic respiratory failure associated with pulmonary hypertension in preterm infants. Study subjects will be administered either inhaled nitric oxide or placebo to determine if there is a change in oxygenation.

NCT ID: NCT00905476 Completed - Clinical trials for Chronic Respiratory Failure

Prognosis in Patients With Chronic Respiratory Failure Receiving Domiciliary Noninvasive Positive Pressure Ventilation (NPPV)

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

The purposes of the present study are (1) to analyze baseline patient characteristics cross-sectionally, (2) to analyze the prognosis and its predictive factors, and (3) to examine longitudinal clinical course in patients with chronic respiratory failure receiving domiciliary NPPV.

NCT ID: NCT00905463 Active, not recruiting - Respiratory Failure Clinical Trials

Prognosis of Lung Transplant Candidates

Start date: April 2009
Phase:
Study type: Observational

The purposes of the study are (1) to analyze the baseline patient characteristics cross-sectionally, (2) to analyze the prognosis and its predictive factors and (3) to examine the longitudinal clinical course in the lung transplant candidates in Japan.

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: NCT00876473 Completed - Clinical trials for Acute Respiratory Failure

Evaluation of Different Continuous Positive Airway Pressure (CPAP) Systems in Patients With Acute Respiratory Failure

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

The aim of this study is to evaluate the performance, the tolerability and the efficacy on gas-exchange of different CPAP (Continuous Positive Airway Pressure) systems.

NCT ID: NCT00875134 Completed - Clinical trials for Respiratory Depression

Testing of the Apnea Prevention Device

Start date: March 2009
Phase: Phase 1/Phase 2
Study type: Interventional

This study is designed to test the ability of a computer-based algorithm to detect and intervene in cases of narcotic-induced respiratory depression.

NCT ID: NCT00871624 Completed - Clinical trials for Acute Respiratory Failure

Efficacy and Safety of Dexmedetomidine During Non-Invasive Positive Pressure Ventilation

Start date: March 2009
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine the efficacy and safety of dexmedetomidine during Non-invasive positive pressure ventilation (NPPV) for patients with acute respiratory failure compared to standard analgesic/sedation practices

NCT ID: NCT00854165 Active, not recruiting - Respiratory Failure Clinical Trials

Lung Transplantation in Respiratory Failure Patients

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

Survival after cadaveric lung transplantation in recipients depended on ventilation support prior to transplantation has been reported to have relative high surgical mortality and morbidity rate. The objectives of this study were to describe the short-term outcomes of bilateral sequential lung transplantation under extracorporeal membrane oxygenation (ECMO) support in a consecutive series of patients who depended on noninvasive and invasive ventilation support preoperatively .

NCT ID: NCT00839033 Terminated - Clinical trials for Amyotrophic Lateral Sclerosis

Evaluation of a Mechanical Device During Acute Respiratory Failure in Patients With Neuromuscular Disorders

Nemucough
Start date: June 2009
Phase: Phase 3
Study type: Interventional

The hypothesis is that a mechanical insufflation-exsufflation (MI-E) is associated with a decrease in the number of intubations and more rapid clinical improvement in children and adults with neuromuscular disease who are admitted for an acute respiratory exacerbation.In this prospective, randomised, multicenter study, 55 patients will be treated with standard treatment and a MI-E, and 55 patients with standard treatment and standard respiratory physiotherapy. The primary objective is the reduction of the number of patients requiring invasive ventilatory support (endotracheal intubation or tracheotomy) in the group treated with MI-E (MI-E group). The main secondary objectives are a reduction in hospital stay and an improvement in clinical condition, dyspnea and respiratory muscle function.