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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT01566968 Completed - Healthy Clinical Trials

Novel Endpoints in Cough Challenge Testing

NEAT
Start date: January 2011
Phase: N/A
Study type: Observational

The sensitivity of a person's cough reflex can be measured by getting them to breathe in (inhale) irritant chemicals. There are different methods by which subjects are asked to inhale these chemicals, either by taking one deep breath in, or by asking them to just continue to take a number of breaths. The purpose of this clinical research study is to see if the coughing responses are different in healthy people and people with respiratory problems that make them cough when they are given these chemicals in these two methods.

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.

NCT ID: NCT01560741 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Telemedicine and Ventilator Titration in Chronic Respiratory Patients Initiating Non-invasive Ventilation

TeleMotiNIV
Start date: July 2012
Phase: Phase 1
Study type: Interventional

The critical nature of respiratory diseases, the continuously increasing prevalence of these conditions, and the subjective perception of patients vis-à-vis their pulmonary function and health status underscore the importance of home telemonitoring. These conditions are critical and necessitate close and regular monitoring that may be achieved at distance using telemonitoring. This study will assess a number of measures both at baseline and post-intervention from a number of domains, including Arterial Blood Gases (ABG), BiPAP-related data, chronic respiratory failure symptoms, health-related quality of life, patients satisfaction and utilization of healthcare resources.

NCT ID: NCT01559116 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Characterization of 24-hour Lung Function Profiles of Inhaled Tiotropium + Olodaterol Fixed Dose Combination in Patients Suffering From Chronic Obstructive Pulmonary Disease

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

The primary objective of the trial is to determine the 24-hour FEV1-time profile of tiotropium + olodaterol FDC, administered once daily by the RESPIMAT Inhaler after 6 weeks of treatment.

NCT ID: NCT01559051 Withdrawn - Clinical trials for Chronic Obstructive Pulmonary Disease

Safety and Efficacy of Adipose Derived Stem Cells for Chronic Obstructive Pulmonary Disease

Start date: March 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The intent of this clinical study is to answer the questions: 1) Is the proposed treatment safe and 2) Is treatment effective in improving the health of patients with human Chronic Obstructive Pulmonary Disease.

NCT ID: NCT01556139 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effectiveness of Respiratory Muscle Training by Spirotiger in Chronic Patients

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

The reduction in effort tolerance as result of a decreased efficiency in ventilation is common both in patients affected by COPD (McKenzie) and chronic heart failure (CHF) (Ribeiro, Frankenstein). One of the most common cause is the reduced respiratory muscle strength and endurance. Some studies have evaluated the effect of a specific training on the muscular strength both in pulmonary (Battaglia, Powell) and cardiac patients (Winkelmann, Chiappa). Moreover, only few studies investigated a specific training for such patients (Koppers, Sherer) because of the complicated equipment needed to prevent hypocapnia. Up to date, portable and economic systems for isocapnic hyperpnea have been developed for respiratory muscle training. Primary aim of the study was to evaluate the effectiveness of the respiratory muscle training -by the technique of the isocapnic hyperpnea- on the effort tolerance and endurance in patients with COPD and CHF Secondary aims were: A.to quantify the number of patients with deficit of respiratory muscles endurance and B.to verify different response of training between COPD and CHF patients

NCT ID: NCT01555593 Completed - Clinical trials for Chronic Obstructive Airway Disease

Effect of Prolonged Decubitus on Nitric Oxide Concentration in Chronic Obstructive Pulmonary Disease

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

- Bronchial obstruction in Chronic Obstructive Pulmonary Disease (COPD) is caused by inflammation of peripheral airways walls. - Neutrophils and other inflammatory mediators Interleukin-6 (IL6), Interleukin-8 (IL8), Interleukin-1 alpha (IL-1 alpha),Interleukin-1beta (IL-1 beta), Tumor Necrosis Factor alfa (TNF-alfa), Reactive Oxygen Species (ROS), Leukotriene B4 (LTB4), Nitric Oxyde (NO) are implicated in the inflammation. - Exhaled NO concentration is usually used to monitor bronchial inflammation - The relationship between decubitus and small airways behaviour is not well understood. - Our hypothesis is that cyclic opening and closure of peripheral airways during decubitus can provoke an inflammatory response which can be monitored by exhaled NO. - Data about these physiopathological aspects is missing in literature.