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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT00138671 Terminated - Diabetes Mellitus Clinical Trials

A One Year Clinical Trial Assessing the Usefulness and Safety of Inhaled Insulin in Diabetics With COPD

Start date: January 2003
Phase: Phase 3
Study type: Interventional

A One Year Clinical Trial Assessing the Usefulness and Safety of Inhaled Insulin in Diabetics with Chronic Obstructive Pulmonary Disease.

NCT ID: NCT00137956 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Endobronchial Valve for Emphysema PalliatioN Trial (VENT) Cost-effectiveness Sub-Study

Start date: December 2004
Phase: Phase 3
Study type: Interventional

The purpose of the VENT Cost-Effectiveness Sub-Study is to gather healthcare utilization and quality of life information on patients enrolled in the VENT study in order to analyze the relative cost-effectiveness of the endobronchial valve implant procedure.

NCT ID: NCT00136006 Active, not recruiting - Clinical trials for Chronic Obstructive Lung Disease

The Vancouver-BOLD Study: The Burden of Chronic Obstructive Lung Disease

Start date: August 2005
Phase: N/A
Study type: Observational

This is a study of the lung health of the population of Vancouver and the extent of, and the risk factors for, chronic obstructive lung disease.

NCT ID: NCT00135252 Terminated - Clinical trials for Lung Diseases, Obstructive

Method of Oxygen Delivery and the Effect on Transcutaneous PaCO2

Start date: August 2005
Phase: Phase 2/Phase 3
Study type: Interventional

Infants of < 1500 grams of birth weight who require a > 1 week mechanical ventilation (breathing machine) or CPAP [continuous positive airway pressure] (oxygen at a high flow through the nose) may have prolonged oxygen requirements. The nasal cannula (oxygen through the nose at a low flow) is the most commonly used method of oxygen administration, despite a lack of data regarding its safety and efficacy. Low birth weight infants are vulnerable to obstruction from secretions and blood, as well as the presence of the nasal cannula. Partially obstructed nostrils greatly increase the work of breathing. Additional potential adverse effects include an increased need for suctioning, increased risk for systemic infection, and inadvertent positive end expiratory pressure (CPAP). No study has been conducted to evaluate the efficacy of the nasal cannula compared to an oxygen hood (plastic "hood" that is placed over the infant's head to provide oxygen) on gas exchange or infection. Among infants who require supplemental oxygen (by either a nasal cannula or an oxygen hood) for clinical indications, objectives the investigators hope to accomplish in a randomized blinded (investigator) trial: Aim 1: To determine the short-term effect of different flows of oxygen by the nasal cannula on transcutaneous PCO2 (PTCO2). Aim 2: To determine, once optimal flow is established in Aim 1, the effect of prolonged (one week) use of a nasal cannula compared to an oxygen hood on PTCO2.

NCT ID: NCT00134979 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Formoterol Certihaler, Tiotropium HandiHaler and Tiotropium HandiHaler in Combination With Formoterol Certihaler in Patients With Stable Chronic Obstructive Pulmonary Disease

Start date: October 2004
Phase: Phase 4
Study type: Interventional

This study is not being conducted in the United States. This study is designed to provide efficacy and safety data for formoterol 10µg twice-a-day (b.i.d.) delivered by the Certihaler in patients with chronic obstructive pulmonary disease (COPD). This study is also designed to compare the efficacy and safety of therapy with formoterol (Certihaler)10µg b.i.d. added to tiotropium (HandiHaler) 18µg once daily (o.d.) compared with tiotropium (HandiHaler) 18µg o.d. monotherapy, and to compare the safety and efficacy of formoterol 10µg b.i.d. (Certihaler) with tiotropium 18µg o.d. (HandiHaler).

NCT ID: NCT00132860 Active, not recruiting - Clinical trials for Pulmonary Disease, Chronic Obstructive

Prophylactic Antibiotic Treatment of Patients With Chronic Obstructive Lung Disease (COLD)

Start date: May 2001
Phase: Phase 4
Study type: Interventional

The purpose of the study is to investigate, in patients with moderate to severe chronic obstructive lung disease, whether intermittent antibiotic treatment leads to: - A slower rate of decline in forced expiratory volume in one second (FEV1); - A reduction in the frequency and severity of exacerbations; - Fewer hospital admissions for chronic obstructive pulmonary disease (COPD); - Lower mortality; - An improved quality of life as compared to a group of placebo treated patients.

NCT ID: NCT00129831 Completed - COPD Clinical Trials

Study to Assess the Safety and Tolerability of Incremental Doses of QAB149 in Adults With Mild-to-moderate Chronic Obstructive Pulmonary Disease (COPD)

Start date: September 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of single doses of QAB149 up to 3000 µg delivered via a single-dose, dry powder inhaler in patients with mild to moderate COPD.

NCT ID: NCT00129584 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Endobronchial Valve for Emphysema Palliation Trial (VENT)

Start date: January 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of the Emphasys Endobronchial Valve (EBV) and procedure (with pulmonary rehabilitation) compared to optimal medical management (with pulmonary rehabilitation) in patients with heterogeneous emphysema.

NCT ID: NCT00128765 Completed - Clinical trials for Lung Diseases, Obstructive

Costs and Effects of Three Modes for Disease Management of Chronic Obstructive Pulmonary Disease in General Practice

Start date: January 2005
Phase: N/A
Study type: Interventional

In this randomized controlled trial, three contemporary modes for chronic obstructive pulmonary disease (COPD) management in Dutch general practices are compared for costs and effects: - usual general practitioner (GP) care (at patient's initiative); - regular practice nurse review; and - integrated self-management education. All three interventions are based on existing guidelines, materials, and field experiences.

NCT ID: NCT00126776 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Veterans Integrated Service Network (VISN) 23 Lung Disease Self Management/Case Management Program

Start date: July 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a program of self management and case management reduces hospitalizations and urgent care visits for patients with chronic obstructive pulmonary disease (COPD).