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Lung Diseases clinical trials

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NCT ID: NCT01574651 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

The Effect of QVA149 on Health Related Quality of Life in Patients With Chronic Obstructive Pulmonary Disease (COPD)

QUANTIFY
Start date: May 2012
Phase: Phase 3
Study type: Interventional

This study will assess the efficacy and safety of QVA149 compared to tiotropium plus formoterol in patients with moderate to severe COPD.

NCT ID: NCT01572948 Completed - COPD Clinical Trials

A Placebo-controlled Trial of Daliresp on Chronic Obstructive Pulmonary Disease (COPD)

Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of the study is to propose that roflumilast is associated with meaningful reductions in biomarkers of pulmonary inflammation and sputum neutrophilia, including confirmation of previously described results, and correlate these findings with improvement in pulmonary function, sputum scores, and quality of life in stable moderate to severe COPD. The investigators aim to demonstrate this regardless of concomitant medication use, including inhaled corticosteroids. Additionally, the investigators hope to provide a mechanistic pathway by which these effects occur.

NCT ID: NCT01572870 Completed - Cystic Fibrosis Clinical Trials

Duplication in CHIT1 Gene and the Risk for Aspergillus Lung Disease in CF Patients

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

Title: Duplication in Chitotriosidase (CHIT1) Gene and the Risk for Aspergillus Lung Disease in CF Patients. Aim: To evaluate the link between CHIT1 duplication in CF patients and the predisposition to ABPA or persistent Aspergillus infection. Patients: 40 CF patients. Design: Observational, single visit. Methods: All patients will be assessed for pulmonary function tests (PFT), sputum cultures, and blood tests for: CHIT1 duplication, immunoglobulin E (IgE) and Eosinophils levels. Part of the patients will be assessed for RAST, skin prick test. Primary outcome measure is the difference in CHIT1 genotyping between the groups.

NCT ID: NCT01572792 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Efficacy, Safety and Tolerability of Two Fixed Dose Combinations of Aclidinium Bromide/Formoterol Fumarate, Aclidinium Bromide, Formoterol Fumarate and Placebo for 28-Weeks Treatment in Patients With Moderate to Severe, Stable Chronic Obstructive Pulmonary Disease (COPD)

Start date: April 2012
Phase: Phase 3
Study type: Interventional

The purpose of this Phase III study is to evaluate the long-term safety and tolerability of two fixed-dose combinations of inhaled aclidinium bromide/formoterol fumarate, aclidinium bromide, formoterol fumarate and placebo in patients with moderate to severe Chronic Obstructive Pulmonary Disease (COPD). Long-term efficacy, pharmacoeconomic and health-related quality of life assessments will also be evaluated. This extension study will include a 28 week treatment period, followed by a four week follow up visit. All patients will remain in the same treatment group as for the lead-in study and continue on one of the four treatment arms or placebo.

NCT ID: NCT01571999 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Study to Assess the Safety and PK of GSK573719 and GSK573719/GW642444(VI) Combination in Healthy Subjects and Subjects With Severe Renal Impairment

Start date: March 29, 2012
Phase: Phase 1
Study type: Interventional

This study will assess the safety and pharmacokinetics of inhaled GSK573719 and GSK573719/vilanterol combination in healthy subjects and in subjects with severe renal impairment. The results of the study will provide guidance on the use of this product in subjects with severe renal impairment.

NCT ID: NCT01570764 Completed - Systemic Sclerosis Clinical Trials

Cyclophosphamide Systemic Sclerosis Associated Interstitial Lung Disease

SCLEROCYC
Start date: January 14, 2013
Phase: Phase 3
Study type: Interventional

By including in this study patients with significant worsening of their lung volumes and / or their DLCO (carbon monoxide diffusing capacity) in the previous year, on the basis of an open retrospective study we recently conducted, we hope to demonstrate that a strategy combining prednisone and intravenous cyclophosphamide therapy is accompanied by an increase in the frequency stabilization / improvement of lung volumes and / or DLCO of patients at 12 months of 15% in the placebo and prednisone cyclophosphamide 50% in cyclophosphamide and prednisone.We also hope to demonstrate significant decrease in the number of patients excluded for failure in the CYC arm as compared to the placebo arm.

NCT ID: NCT01566773 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

PT001 MDI Versus Spiriva® in Patients With Moderate to Severe COPD

Start date: March 2012
Phase: Phase 2
Study type: Interventional

The overall objective of this study is to determine an optimal dose and dosing regimen of PT001 MDI for further evaluation in later stage studies.

NCT ID: NCT01566604 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Efficacy, Safety and Tolerability of NVA237 in Patients With Chronic Obstructive Pulmonary Disease

GLOW7
Start date: March 2012
Phase: Phase 3
Study type: Interventional

This study will assess of the efficacy and safety of a once-daily, 50µg inhalation of NVA237 in moderate to severe chronic obstructive pulmonary disease (COPD) patients over 26 weeks treatment.

NCT ID: NCT01564953 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Vitamin D, Magnesium and Calcium in Chronic Obstructive Pulmonary Disease (COPD)

Start date: February 2012
Phase: N/A
Study type: Observational

This study will investigate the serum level of vitamin D, magnesium and calcium in patients with chronic obstructive pulmonary disease (COPD) in order to evaluate the impact of vitamin D, magnesium and calcium on lung function in COPD-patients.

NCT ID: NCT01561625 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Signaling Pathway Activation After Exercise in Patients With Chronic Obstructive Pulmonary Disease

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

Muscle weakness and atrophy are important consequences of chronic obstructive pulmonary disease (COPD). Although resistance exercises increase strength and muscle mass in patients with COPD, the response to training appears to be suboptimal in these individuals. A dysregulation in the signaling pathways involved in the regulation of muscle mass could play an important role in this phenomenon. Hypothesis: Proteins involved in muscle mass regulation will be less activated in the quadriceps of patients with COPD following the acute bout of resistance training exercise compared to healthy age-matched controls.