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Lung Diseases clinical trials

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NCT ID: NCT01155310 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Efficacy of Helium/Oxygen Compared to Air/Oxygen in Severe Exacerbation of Chronic Obstructive Pulmonary Disease (COPD)

ECHO/ICU
Start date: May 2010
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to evaluate the efficacy of Helium/Oxygen (He/O2) 78%/22% compared to a conventional Air/O2 mixture in reducing endotracheal intubation rate and mortality in patients with severe hypercapnic exacerbations of Chronic Obstructive Pulmonary Disease (COPD) during their index Intensive/Intermediate Care Unit (ICU) stay.

NCT ID: NCT01101126 Terminated - Asthma Clinical Trials

Disease Management in Asthma or Chronic Obstructive Pulmonary Disease (COPD) Patients

ACDM-Maccabi
Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether disease management program is effective in preventing acute exacerbations in patients with unstable chronic obstructive pulmonary disease (COPD) or asthma.

NCT ID: NCT01077778 Terminated - Pulmonary Embolism Clinical Trials

Magnetic Resonance Diagnosis of Pulmonary Embolism

IRM-EP
Start date: March 2007
Phase: N/A
Study type: Observational

- The purpose of this study is to evaluate the diagnostic accuracy of thoracic magnetic resonance imaging with gadolinium-enhanced, unenhanced and perfusion sequences in patients with clinically suspected acute pulmonary embolism - Thoracic CT angiography (CTA) will serve as reference standard - Result of MRI will not interfere with patients' management - Untreated patients with negative CTA will have 3-month follow-up to verify they were free of thrombose-embolic disease

NCT ID: NCT01068184 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

A Study to Assess Safety, Tolerability and Pharmacokinetics of of AZD6553 in Healthy Volunteers and Patients With Chronic Obstructive Pulmonary Disease (COPD)

Start date: February 2010
Phase: Phase 1
Study type: Interventional

AZD6553 is a new drug being developed as a possible treatment for patients with chronic obstructive pulmonary disease (COPD). COPD refers to chronic bronchitis and emphysema, a pair of two commonly co-existing diseases of the lungs in which the airways become inflamed and the small airsacs of the lungs become damaged. This leads to a limitation of the flow of air to and from the lungs causing shortness of breath. In contrast to asthma, the limitation of airflow is poorly reversible and usually gets progressively worse over time. There is an urgent medical need for therapies that could slow disease progression by targeting the underlying mechanisms associated with the changes in the lungs in patients with COPD. AZD6553 acts by reducing the activity of a protease found to be involved in the disease process in COPD. AZD6553 is being developed as a novel oral treatment to control the symptoms and exacerbations of COPD, and reduce the progression and severity of the disease. The purpose of this research study is to determine how safe and well-tolerated AZD6553 is and how much AZD6553 enters blood circulation by collecting blood and urine samples during the study. We are also investigating what AZD6553 is broken down into, when given orally, how much of the drug is cleared from the body via the kidneys, and the effect of taking the drug after food. This will all be done by analysis of blood and urine samples taken at various point during the study.

NCT ID: NCT01068145 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Two-Part Study to Evaluate the Dose Response of SCH 527123 on Sputum Neutrophilia Following Ozone Challenge in Healthy Subjects and Chronic Obstructive Pulmonary Disease (COPD) Patients (P05567 AM7)

Start date: February 2010
Phase: Phase 1
Study type: Interventional

Trial to evaluate the dose response of SCH 527123 in reducing inflammation from an ozone-induced sputum neutrophilia in both healthy subjects and subjects with COPD.

NCT ID: NCT01061671 Terminated - Clinical trials for Pulmonary Disease, Chronic Obstructive

Simvastatin Therapy for Moderate and Severe COPD

STATCOPE
Start date: March 2010
Phase: Phase 3
Study type: Interventional

To determine the effect of daily administration of 40 mgms simvastatin taken for at least 12 months (range 12-36 months) on the frequency of exacerbations of chronic obstructive lung disease (COPD) in patients with moderate to severe COPD who are prone to exacerbations and do not have other indications for statin treatment.

NCT ID: NCT01026207 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Portable Monitoring Device for the Diagnosis of Sleep Apnea in Patients With Chronic Obstructive Pulmonary Disease

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

Introduction: The prevalence of overlap between Chronic Obstructive Pulmonary Disease (COPD) and Obstructive Sleep Apnea Syndrome (OSAS) is around 10%. This overlap syndrome is an important issue because is related to nocturnal desaturation and its complications. The use of portable monitoring devices (PM) for the diagnosis of OSAS was recently accepted as an alternative to full-night polysomnography (PSG). However, there are not studies evaluating the PM recording in COPD patients to detect or exclude OSAS. Objective: To evaluate if a PM (Stardust®, Respironics, Inc, USA) could accurately measure the apnea-hypopnea index (AHI) in COPD patients with a suspicion of OSAS.

NCT ID: NCT01021202 Terminated - Clinical trials for Pulmonary Disease, Chronic Obstructive

Timing of Dilation Tracheostomy in Mechanically Ventilated Chronic Obstructive Pulmonary Disease (COPD) Patients

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

The purpose of this study is: - to evaluate the optimal time-point for percutaneous dilation tracheostomy in COPD patients in terms of duration on mechanical ventilation, length of stay on ICU and mortality; - to evaluate the rate of infections and infectious complications of tracheostomized COPD patients; - to evaluate the spectrum of pathogens in tracheostomized and intubated COPD patients; - to evaluate the amount of sedatives used in mechanically ventilated COPD patients; - to assess the quality of life in COPD patients tracheostomized after 3 or after 10 days.

NCT ID: NCT01016951 Terminated - Healthy Clinical Trials

A Multiple Ascending Dose Study With AZD9164 Given for 13 Days in Healthy Male and Female Subjects and in Patients With Chronic Obstructive Pulmonary Disease

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

The purpose of this study is to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of inhaled AZD9164 following administration of multiple ascending doses in healthy male and female subjects and COPD patients.

NCT ID: NCT00966823 Terminated - Lung Disease Clinical Trials

Fetal Tracheal Balloon Study in Diaphragmatic Hernia

Start date: September 2008
Phase: Phase 2
Study type: Interventional

The purpose of this phase 2 limited study is to examine whether prenatal intervention correct the lung underdevelopment associated with severe diaphragmatic hernia.