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Lung Diseases clinical trials

View clinical trials related to Lung Diseases.

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NCT ID: NCT01619657 Completed - Clinical trials for Cystic Fibrosis Lung Disease

Preventive Inhalation of Hypertonic Saline in Infants With Cystic Fibrosis

PRESIS
Start date: June 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess whether 6% hypertonic saline (HS) is a safe and effective preventive therapy in newborns and infants with cystic fibrosis (CF).

NCT ID: NCT01619540 Completed - COPD Exacerbation Clinical Trials

Valsalva Manœuvre in the Diagnosis of Left Ventricular Failure in Chronic Obstructive Pulmonary Disease Exacerbation

Start date: May 2011
Phase: N/A
Study type: Interventional

Left ventricular failure (LVF) is a common cause of acute exacerbation of chronic obstructive pulmonary disease (AECOPD). This association is frequently underestimated with regard to the difficulty of clinical diagnosis . The investigators expect that Valsalva Maneuver (VM) could be useful in this issue.

NCT ID: NCT01618721 Terminated - Clinical trials for Lung Disease, Interstitial

Detection and Characterization of Pulmonary Disease by Transthoracic Doppler (TTD)

Start date: December 2011
Phase: N/A
Study type: Observational

The study seeks to characterize data obtained from patients with a variety of lung diseases using ultrasound Doppler signals obtained from lung tissue. A standard ultrasound device in a Doppler mode is placed on the chest wall and the unique software the investigators have developed analyzes the signals reflected from within the lung. On the basis of of pilot studies performed previously the investigators expect to receive different signals from different diseases that will enable diagnosis of different lung diseases.

NCT ID: NCT01616745 Recruiting - Clinical trials for Nontuberculosis Mycobacterial Lung Disease

Phenotypic Clinical, and Genetic Characteristics of Patients With Nontuberculosis Mycobacteria

Korean NTM
Start date: July 2011
Phase: N/A
Study type: Observational

The purpose of this study is to elucidate phenotypic, clinical, and genetic characteristics of Korean Nontuberculosis Mycobacteria (NTM) patients.

NCT ID: NCT01615783 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Clinical and Economic Burden of Patients With Chronic Obstructive Pulmonary Disease in a Medicaid Population

Start date: November 2010
Phase: N/A
Study type: Observational

Reports suggest that the Medicaid population includes a higher percentage of smokers than the general population. A high prevalence of smokers in a population is likely to lead to a higher burden of chronic obstructive pulmonary disease (COPD). Few studies have evaluated the economic burden of COPD in a Medicaid population. The objective of this observational, retrospective cohort study is to estimate the economic burden of COPD in subjects with a COPD diagnosis who are enrolled in Medicaid and are receiving maintenance treatment covered by Medicaid. Specifically, the null hypothesis for the primary outcome measure is that no difference is observed in all-cause costs between subjects with and without COPD. The test hypothesis is that there is a difference in all-cause costs between subjects with and without COPD. Secondary outcomes to be evaluated include all-cause resource use and COPD-related costs for the COPD cohort. The study uses a medical and pharmacy administrative claims database called MarketScan Medicaid Database that contains the medical, surgical, and prescription drug experience of nearly 7 million Medicaid recipients. This analysis will use data from 8 states.

NCT ID: NCT01615484 Completed - Cystic Fibrosis Clinical Trials

Ex-vivo Perfusion and Ventilation of Lungs Recovered From Non-Heart-Beating Donors to Assess Transplant Suitability

Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this research study is to learn about the safety of transplanting lungs obtained from non-heart-beating donors (NHBDs) that have been ventilated (attached to a breathing machine or ventilator to deliver oxygen) and perfused with a lung perfusion solution (Steen solution™, made by Vitrolife). This ventilation and perfusion will be done outside the body (ex-vivo) in a modified cardiopulmonary bypass circuit (the kind of device used routinely during most heart surgeries). The purpose of performing ex-vivo perfusion and ventilation is to learn how well the lungs work, and whether they are likely safe to transplant.

NCT ID: NCT01614951 Completed - Clinical trials for Chronic Obstructive Lung Disease

The Pulmonary Protection Trial

Start date: July 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate whether patients with a preoperative reduced pulmonary function have a better preserved oxygenation capacity after open heart surgery, using either pulmonary perfusion or pulmoplegia compared with TAVI and the control-group with standard ECC (Extra Corporal Circulation).

NCT ID: NCT01613326 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Efficacy, Safety, and Tolerability of NVA237 Compared to Tiotropium in Patients With Chronic Obstructive Pulmonary Disease (COPD)

GLOW5
Start date: June 2012
Phase: Phase 3
Study type: Interventional

This study compared the efficacy and safety of NVA237 with tiotropium in patients with moderate to severe COPD. Tiotropium belongs to the same drug class as NVA237.

NCT ID: NCT01612793 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Vagus Nerve Stimulation for Management of Bronchoconstriction in Patients Hospitalized With COPD Exacerbations

Start date: October 2012
Phase:
Study type: Observational

This study will look at the safety, improving symptoms and decreasing the length of stay of patients admitted to the hospital with COPD.

NCT ID: NCT01611870 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

AVAPS-AE Algorithm in Chronic Obstructive Pulmonary Disease (COPD)Patients

AVAPS-AE COPD
Start date: May 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the performance of AVAPS AE therapy in COPD patients during nocturnal ventilation.