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Lung Disease clinical trials

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NCT ID: NCT01107054 Completed - Pulmonary Disease Clinical Trials

A Study to Investigate the Effects of PF00610335 on the QT/QTC Interval in Healthy Volunteers

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

A study to determine the cardiovascular effects of PF00610335 in healthy volunteers.

NCT ID: NCT01090804 Unknown status - Lung Disease Clinical Trials

The Effectiveness of BreatheMAX Breathing Device on Secretion Clearance

ESMOSC
Start date: August 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determined effects of BreatheMAX on secretion clearance.

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.

NCT ID: NCT00934778 Completed - Lung Cancer Clinical Trials

Minimally Invasive Endoscopy in Diffuse Lung Disease

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

We want to compare 2 new systems for obtaining very detailed images of the smallest airways, in the hope that they can be used to provide useful information about lung diseases without the need for invasive tests. Two new systems have been developed for use down the bronchoscope, which provide video imaging of the smallest airways, each system looking at a different aspect of the structure of the airway walls. In principal, this method could provide useful information which may reduce the need for a surgical lung biopsy. We will therefore be assessing the value of the additional information obtained with these two new systems. The purpose of this research project is to gather information using both systems to gain a greater understanding of the tissue characteristics of various diseases without the need for a biopsy.

NCT ID: NCT00843414 Completed - Lung Disease Clinical Trials

Immunological Characterization of Bronchoalveolar Cells in Normals

Start date: March 1978
Phase: N/A
Study type: Observational

To obtain the monocytes (white blood cells) from normal volunteers for the purpose of studying how proteins, fats, carbohydrates, as well as RNA and DNA for gene expression, relate to immunity. This information will be compared to other studies in patients with lung diseases such as Emphysema, Sarcoidosis, and Interstitial Pulmonary Fibrosis.

NCT ID: NCT00837681 Completed - Lung Disease Clinical Trials

Pulmonary Complications of Hematopoietic Stem Cell Transplantation

Start date: October 2005
Phase: N/A
Study type: Observational

The purpose of this study is to determine risk factors associated with the development of lung disease after hematopoietic stem cell transplantation. Depending on the results and findings of this study, it may be possible to predict who is at higher risk of serious complications and ultimately develop therapies to prevent or treat this lung disease.

NCT ID: NCT00818025 Completed - Lung Disease Clinical Trials

Comparing Methods for Tracking Health Information at Home After Lung Transplant

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

The purpose of this randomized controlled trial is to test the efficacy of a novel intervention, Pocket PATH (Personal Assistant for Tracking Health) for promoting self-care agency, self-care behaviors, and transplant-related health.

NCT ID: NCT00817167 Completed - Lung Disease Clinical Trials

Added Value of inReach Software on Performance Characteristics of Standard Bronchoscopy

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

The study is aimed to evaluate and describe the added value of inReach planning software on performance characteristics of standard bronchoscopy.

NCT ID: NCT00760071 Completed - Cystic Fibrosis Clinical Trials

Magnetic Resonance Imaging (MRI) for Early Diagnosis of Cystic Fibrosis (CF)

Start date: July 2006
Phase: N/A
Study type: Observational

In patients with Cystic Fibrosis (CF) the clinical course of lung disease is crucial for individual prognosis and life expectancy. Imaging modalities are important in the assessment of follow up of structural lung changes and monitoring of pulmonary complications in CF. Although high resolution computed tomography (HRCT) is the accepted gold standard for evaluation of morphological lung changes in CF, chest-X-ray is widely used as standard imaging procedure for assessment and follow up in these young patients due to less radiation exposure. Magnetic resonance imaging (MRI) has not been used for lung imaging in CF so far. Studies from the 80's and early 90's were not able to show any impact for the use of MRI in CF. Due to recent technical developments MRI of the lung became possible. Our study group was able to show that MRI is a competitive imaging modality for evaluating changes of the CF-lung in comparison to the gold standard (HRCT). So far only patients from the age of 6-7 years were examined. According to recent studies CF is a disease which starts in utero. Therefore it can lead to extensive pulmonary changes even in infants and young children. In this age group lung function testing is difficult and not broadly available. An early optimized therapy is crucial for the long term course and outcome of the pulmonary disease. The aim of this study is to evaluate morphological and functional MRI for early diagnosis of lung changes in children (0-6 years) with CF.

NCT ID: NCT00751309 Terminated - Lung Disease Clinical Trials

Lung Allograft Rejection Gene Expression Observational (LARGO) Study

LARGO
Start date: April 2004
Phase: N/A
Study type: Observational

The objective of the LARGO Study protocol is to collect peripheral blood samples, select associated lung biopsy pathology slides, and clinical data from lung transplant recipients to perform molecular analyses in association with the study endpoints. The primary objective is to use gene expression profiling of peripheral blood mononuclear cells to differentiate between the absence and presence of acute cellular rejection. The secondary objectives are to use other genomic and proteomic technologies to analyze RNA and protein in blood samples in relation to related clinical conditions. The overall goal is to apply novel molecular insights in the development of non-invasive molecular diagnostic tests for lung transplantation.