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Pulmonary Edema clinical trials

View clinical trials related to Pulmonary Edema.

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NCT ID: NCT00439075 Completed - Clinical trials for Acute Cardiogenic Pulmonary Edema

OUT-OF-HOSPITAL CPAP STUDY

Start date: October 2006
Phase: Phase 4
Study type: Interventional

Evaluate efficacy and safety of CPAP in a randomised standard treatment controlled study, in out-of-hospital patients with acute cardiogenic pulmonary edema.

NCT ID: NCT00390442 Completed - Clinical trials for Cardiogenic Pulmonary Edema

Out-of-Hospital CPAP for Severe Cardiogenic Pulmonary Edema

Start date: n/a
Phase: Phase 3
Study type: Interventional

In cardiogenic pulmonary edema, Continuous Positive Airway Pressure (CPAP) added to medical treatment improves outcome. The present study was designed to assess the benefit of CPAP as a first line treatment of cardiogenic pulmonary edema in the out-of-hospital environment.

NCT ID: NCT00375154 Withdrawn - Clinical trials for ARF Secondary to COPD Exacerbation

HERMES STUDY: Study on the Feasibility and Efficiency of Noninvasive Positive-Pressure Ventilation (NPPV) in Prehospital Care

Start date: August 2006
Phase: N/A
Study type: Interventional

The purpose of this study is determine if NPPV can be performed in a pre-hospital setting very early after onset of dyspnea with a similar benefit in need of intubation and mortality as in previous study in hospital context and if early NPPV intervention have a real, rather standard medical therapy, value, both on objectively measured parameters and on patient's clinical status.

NCT ID: NCT00331656 Not yet recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Comparative Study of Non-Invasive Mask Ventilation vs Cuirass Ventilation in Patients With Acute Respiratory Failure.

Start date: June 2008
Phase: Phase 4
Study type: Interventional

Non-invasive ventilation has become increasingly important in the management of patients with acute respiratory failure. One of its major goals is to prevent the need for invasive ventilation, which is associated with numerous complications. This study compares the usefulness and safety of two noninvasive techniques which are used in Medical practice: Noninvasive positive pressure ventilation using a face mask and extrathoracic biphasic ventilation using a cuirass. Each of these techniques has advantages and disadvantages and both may not suit all patients. It is therefore important to compare the two in terms of effectiveness in preventing invasive ventilation and their side effects profile, so that we can improve our understanding and expertise in the treatment of patients in respiratory failure.

NCT ID: NCT00310401 Completed - Pulmonary Edema Clinical Trials

The Effect of Nebulized Albuterol on Donor Oxygenation

Start date: April 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test the effectiveness of albuterol versus placebo with the following specific aims: a) Treatment of brain dead organ donors with albuterol will reduce pulmonary edema, improve donor oxygenation, and increase the number of lungs available for transplantation, b) Developing a blood test to predict the development of primary graft dysfunction in lung transplant recipients, and c) treating brain dead organ donors with albuterol will decrease markers of primary graft dysfunction and lead to improved lung transplant recipient outcomes and to higher rates of lungs suitable for transplantation.

NCT ID: NCT00289276 Completed - Heart Diseases Clinical Trials

FAST (Fluid Accumulation Status Trial)

Start date: November 2003
Phase: N/A
Study type: Interventional

Heart failure is a progressive disease that decreases the pumping action of the heart. This may cause a backup of fluid in the heart and may result in heart beat changes. Using very low electrical pulses that travel across the inside of the chest cavity, thoracic fluid status monitoring (OptiVolâ„¢) can measure the level of resistance to the electrical pulses, which indicates the level of fluid in the chest. The purpose of this study is to collect information related to fluid build up in the chest of subjects with heart failure.

NCT ID: NCT00274430 Completed - Clinical trials for High Altitude Pulmonary Edema

Prevention of High Altitude Pulmonary Edema

Start date: July 2003
Phase: Phase 1/Phase 2
Study type: Interventional

A double-blind placebo controlled study - To compare the effect of tadalafil and dexamethasone versus placebo on Ppa and pulmonary edema formation in subjects susceptible to HAPE. - To investigate the effect of dexamethasone on alveolar fluid clearance, as assessed by measurement of the nasal potential difference, and prevention of HAPE. - To investigate the effect of the tadalafil and dexamethasone versus placebo on the dynamic CBF autoregulation properties and on the development of AMS in HAPE susceptible subjects.

NCT ID: NCT00213681 Completed - Clinical trials for Severe Acute Cardiogenic Pulmonary Edema

CPAP Versus Bilevel Pressure Support Ventilation in Cardiogenic Pulmonary Edema

Start date: November 2002
Phase: Phase 3
Study type: Interventional

To evaluate whether bilevel positive airway pressure more rapidly improves ventilation than continuous positive airway pressure (CPAP) in patients with acute pulmonary edema. CPAP is delivered via a simple device connected to oxygen.

NCT ID: NCT00043836 Completed - Dyspnea Clinical Trials

The DIAMOND Study: Distensibility Improvement And Remodeling in Diastolic Heart Failure

Start date: July 2002
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test the hypothesis that treatment with oral ALT-711 twice daily for 16 weeks will improve aortic distensibility, exercise tolerance, and quality of life in elderly patients with isolated diastolic heart failure (DHF), and that the improvements in exercise tolerance will correlate with the improvements in aortic distensibility.

NCT ID: NCT00014989 Completed - Cerebral Palsy Clinical Trials

Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)

BEAM
Start date: December 1997
Phase: Phase 3
Study type: Interventional

As many more premature infants survive, the numbers of these infants with health problems increases. The rate of cerebral palsy (CP) in extremely premature infants is approximately 20%. Magnesium sulfate, the most commonly used drug in the US to stop premature labor, may prevent CP. This trial tests whether magnesium sulfate given to a woman in labor with a premature fetus (24 to 31 weeks out of 40) will reduce the rate of death or moderate to severe CP in the children at 2 years. The children receive ultrasounds of their brains as infants and attend three follow-up visits over two years to assess their health and development.