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Lung Diseases clinical trials

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NCT ID: NCT01486186 Not yet recruiting - Clinical trials for Pulmonary Disease, Chronic Obstructive

Effect of Traditional Chinese Medicine on Outcomes in Patients With Mild/Moderate Chronic Obstructive Pulmonary Disease

Start date: December 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is evaluate the effects and safety of Traditional Chinese medicine for prevention and management of mild/moderate chronic obstructive pulmonary disease (COPD).

NCT ID: NCT01483625 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Tiotropium (18mcg) in Chronic Obstructive Pulmonary Disease (COPD) Patients With a Respiratory Infection

Start date: November 2011
Phase: Phase 4
Study type: Interventional

The aim of the study is to investigate whether the early introduction of maintenance bronchodilator therapy during an acute symptomatic episode of the disease shows benefits on the recovery of symptoms. It also represents an opportunity to identify COPD patients earlier in their disease state and start maintenance therapy, if appropriate.

NCT ID: NCT01483534 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Innovative Pulmonary Solutions (IPS) System for Targeted Lung Denervation

IPS-I
Start date: October 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety of Targeted Lung Denervation Therapy (or TLD TherapyTM) in patients suffering from COPD. Technical feasibility of the IPS SystemTM will also be evaluated through confirmation of successful application of TLD Therapy.

NCT ID: NCT01482000 Not yet recruiting - Clinical trials for Pulmonary Disease, Chronic Obstructive

Does Pulmonary Daoyin of China Give Additional Benefit Over Usual Therapy in Management of Stable Chronic Obstructive Pulmonary Disease?

Start date: November 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the exercise capacity and pulmonary function test parameters of Chronic Obstructive Pulmonary Disease (COPD) patients who underwent usual care with and without pulmonary daoyin therapy of China in community.

NCT ID: NCT01481506 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Multiparametric Telemonitoring In Elderly People With Chronic Obstructive Pulmonary Disease

SweetAge
Start date: January 2010
Phase: N/A
Study type: Interventional

Chronic obstructive pulmonary disease (COPD) determines an important risk of disability and disease-related need of care. Selected interventions were able to reduce the number and the severity of exacerbations. Telemedicine has also been proposed for this purpose. Current evidences, however, are scant. The investigators present a randomized, parallel-group trial of a multiparametric remote monitoring system to test its ability to improve early exacerbation detection rates and impact on clinical outcomes.

NCT ID: NCT01480882 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Efficacy and Safety Study of a Percussion Device to Mobilise Sputum From Respiratory Passage

LEGA
Start date: December 2011
Phase: Phase 2/Phase 3
Study type: Interventional

A Malaysian company by name Formedic Technologies SDN BHD has devised a hand held machine which is supposed to mimic the chest percussion performed by professional physiotherapist to mobilize sputum through the respiratory passage. The aim of this study is to compare the effectiveness and safety of this mechanical percussion device in the treatment of airway clearance with conventional chest physiotherapy carried out by qualified physiotherapists in patients suffering from bronchiectasis or Chronic obstructive Pulmonary disease (COPD).

NCT ID: NCT01480661 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Evaluation With CT Scan of Possible Changes in Airways After Treatment With Daxas® in Severe Chronic Obstructive Pulmonary Disease Patients

Start date: December 2011
Phase: Phase 4
Study type: Interventional

In this study the possible changes in airway geometry and function induced by 6 month oral treatment with Daxas® (roflumilast) will be evaluated. The use of functional respiratory imaging (FRI) on the phenotyping of chronic obstructive pulmonary disease (COPD) patients will be examined. The study population consists of 40 severe COPD patients, global initiative for chronic obstructive lung disease (GOLD) stages III until IV. Imaging parameters will be assessed and the correlation with lung function and health related quality of life will be checked before and after treatment.

NCT ID: NCT01478646 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

The Effect of Reflective Breathing Therapy Compared With Conventional Breathing Therapy in Patients With Chronic Obstructive Pulmonary Disease (COPD) III-IV

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

The purpose of this study is to determine whether different types of breathing therapies in patients with COPD III-IV decrease dyspnea and increase activity.

NCT ID: NCT01475292 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

A Study to Investigate How Safe and Well Tolerated RV568 is in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Start date: November 2011
Phase: Phase 2
Study type: Interventional

RV568 is being developed as a possible treatment of diseases such as smoking related lung disease (also known as Chronic Obstructive Pulmonary Disease - COPD) and asthma. The main purpose of this study is to examine the safety of RV568 in COPD patients. Two dose strengths of RV568 and a placebo will be tested in this study, which will be given by inhaling a liquid suspension from a nebuliser once a day for 2 weeks.

NCT ID: NCT01475045 Completed - Asthma Clinical Trials

ANASA (Patients' Satisfaction With Pulmonary Diseases' Treatment)

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

The aim of the study is to compare patients' satisfaction from the use of three different inhalation devices by using the FSI-10 questionnaire