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Lung Disease clinical trials

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NCT ID: NCT00704171 Completed - Lung Disease Clinical Trials

PleuraSeal Post Market Study (Europe)

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

To further characterize the PleuraSeal Sealant System as compared to standard of care (sutures and staples only) in subjects undergoing an elective pulmonary lobectomy and segmentectomy via open thoractomy.

NCT ID: NCT00618852 Recruiting - Lung Disease Clinical Trials

Using Furosemide to Prevent Fluid Overload During Red Blood Cell Transfusion in Neonates

Start date: January 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the effects of intravenous furosemide on cardio-respiratory performance in neonates receiving a packed red blood cell (PRBC) transfusion who are considered at high risk of volume overload.

NCT ID: NCT00551642 Completed - Lung Disease Clinical Trials

Safety and Efficacy Study of Nitric Oxide for Inhalation on Chronic Lung Disease in Premature Babies

Start date: May 29, 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of inhaled nitric oxide to reduce the risk of chronic lung disease in pre-term infants with respiratory distress, and to assess the long-term effects of the therapy on the development of these children over 7 years of clinical follow-up.

NCT ID: NCT00504738 Completed - Asthma Clinical Trials

Lung Disease Collection (Qatar): Evaluation of the Lungs of Individuals With Lung Disease

Q-LD
Start date: April 2006
Phase: N/A
Study type: Observational

The purpose of this protocol is to obtain biologic samples from the blood and lungs from patients with lung diseases in order to study the causes and indications of these disorders, learn how these lung disease manifest and progress, and how the lung disease can be treated.

NCT ID: NCT00455767 Completed - Inflammation Clinical Trials

Safety and Efficacy Study of Depelestat in Acute Respiratory Distress Syndrome (ARDS) Patients

Start date: July 2006
Phase: Phase 2
Study type: Interventional

The study is aimed to assess safety of Depelestat treatment, as well as efficacy on prevention and treatment of alveolar inflammation in early pulmonary fibrosis in patients suffering from persistent Acute Respiratory Distress Syndrome.

NCT ID: NCT00315263 Completed - Respiratory Failure Clinical Trials

Genomics, Single Nucleotide Polymorphisms (SNPs), and Clinical Neonatology

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

This research seeks to establish a neonatal DNA Tissue Bank to find out if differences in small segments of DNA predispose babies to Chronic Lung Disease (CLD), Periventricular Brain Injury (PVI), Necrotizing Enterocolitis (NEC), or Hypoxic Respiratory Failure (HRF).

NCT ID: NCT00224198 Completed - Asthma Clinical Trials

Evaluation of the Lungs of Individuals With Lung Disease

Start date: January 2004
Phase: N/A
Study type: Observational

The purpose of this protocol is to obtain biologic materials from the blood and lungs from patients with lung disease in order to develop an understanding of the etiology and pathogenesis of these disorders. General admission criteria for this project will require at least one of the following: (1) symptoms consistent with pulmonary disease; (2) chest X-ray consistent with lung disease; (3) pulmonary function tests consistent with lung disease; (4) lung biopsy consistent with lung disease; (5) family history of lung disease; and (6) patients with diseases of organs with known association with lung disease.

NCT ID: NCT00139152 Completed - Lung Disease Clinical Trials

Non-invasive Ways to Evaluate Lung Disease After Treatment With Xolair

Start date: September 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to study the effects of Xolair using non-invasive techniques from the expired gas of patients with moderate to severe allergic asthma.

NCT ID: NCT00131274 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Gleevec Idiopathic Pulmonary Fibrosis (IPF) Study

Start date: April 2003
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of the study is to evaluate the safety and efficacy of Gleevec (imatinib mesylate) in the treatment of idiopathic pulmonary fibrosis (IPF).

NCT ID: NCT00077909 Recruiting - Pneumonia Clinical Trials

Study of Lung Proteins in Patients With Pneumonia

Start date: February 20, 2004
Phase:
Study type: Observational

This study will examine the different types of proteins present in the lungs of patients with pneumonia to explore the causes of different types of the disease. Pneumonia is a condition that causes lung inflammation AND is often caused by an infection. It is usually diagnosed by lung x-rays and listening to the chest with a stethoscope. This method can diagnose pneumonia, but it does not provide information on the cause of the inflammation - information that might be helpful in guiding treatment. This study will measure proteins in the lungs of patients to see if certain proteins are associated with specific forms of pneumonia, and can thus serve as biomarkers for disease. Patients undergoing diagnostic bronchoscopy at the NIH Clinical Center may participate in this study. Patients will undergo bronchoscopy and bronchoalveolar lavage as scheduled for their medical care. For this procedure, the patient's mouth and throat are numbed with lidocaine; a sedative may be given for comfort. A thin flexible tube called a bronchoscope is advanced through the nose or mouth into the lung airways to examine the airways carefully. Saline (salt water) is then injected through the bronchoscope into the air passage, acting as a rinse. A sample of fluid is then withdrawn for microscopic examination. Researchers in the current study will use some of the fluid obtained from the lavage to examine for protein content. In addition to the bronchoscopy and bronchoalveolar lavage, participants will have about 2 tablespoons of blood drawn to compare blood test results with the results of the lung washings. Patients' medical records will be reviewed to obtain information on past medical history, current medical treatment, vital signs, and results of x-ray tests.