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Sponsored by: |
Fondazione Salvatore Maugeri |
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Information provided by: | Fondazione Salvatore Maugeri |
ClinicalTrials.gov Identifier: | NCT00783250 |
The aim of this study is to assess the effects on respiratory mechanics of one "classical" short-term bronchodilator (i.e. salbutamol) vs placebo, and to verify the hypothesis that the addition of another bronchodilator (i.e. anticholinergic) may induce a further improvement on the work of breathing of stable COPD patients.
Condition | Intervention | Phase |
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Chronic Obstructive Pulmonary Disease |
Drug: Salbutamol + Tiotropim Drug: Placebo + Tiotropium |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study |
Official Title: | Effect of Bronchodilators on Respiratory Mechanics in COPD Patients With Poor Reversibility |
Estimated Enrollment: | 20 |
Study Start Date: | September 2008 |
Estimated Study Completion Date: | August 2009 |
Estimated Primary Completion Date: | June 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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Salbutamol+Tiotropium: Experimental
Salbutamol will be given at the dose of 400 micrograms and Tiotropium at the dose of 18 micrograms
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Drug: Salbutamol + Tiotropim
Salbutamol 400 micrograms + Tiotropim 18 micrograms
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placebo + Tiotropium: Placebo Comparator
Placebo using MDI + administration of Tiotropium after 20 minutes
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Drug: Placebo + Tiotropium
Placebo via MDI + Tiotropium 18 micrograms
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Studies with long-acting b2-agonists in COPD patients who poorly respond to routine airways obstruction reversibility tests with forced expiratory manoeuvres, such as forced expiratory volume in one second (FEV1), are scarce. Such studies, however, seem to show favourable effects on clinica parameters. This may explain the subjective improvements and changes in quality of life with long-acting b2-agonists in patients with COPD. The lack of effect on forced expiration tests may be due to early airway collapse and subsequent airflow decline causing underestimation of the existing bronchodilatory effects located more peripherally in the respiratory tract, where the major site of resistance is located in obstructive lung disease.
We therefore design a study aimed to assess the short term effects of one short-acting beta2-agonist vs placebo, and the effects of an additional and sequential administration of a different bronchodilator, like tiotropium bromide (anticholinergic agent) on the work of breathing, and its components (i.e. lung resistances and compliance)of COPD patients with poor reversibility assessed using the classical Pulmonary Function Tests.
Ages Eligible for Study: | 20 Years to 85 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Stefano Nava, MD | 0382 592806 | stefano.nava@fsm.it |
Contact: Annalisa Carlucci, MD | 0382 592801 | annalisa.carlucci@fsm.it |
Italy, PV | |
Respiratory Unit Fondazione S.Maugeri | Recruiting |
Pavia, PV, Italy, 27100 | |
Contact: Stefano Nava, MD 0382 592806 stefano.nava@fsm.it | |
Contact: Annalisa Carlucci, MD 0382 592801 annalisa.carlucci@fsm.it | |
Principal Investigator: Stefano Nava, MD |
Responsible Party: | Fondazione S.Maugeri ( Stefano Nava ) |
Study ID Numbers: | 350 |
Study First Received: | October 30, 2008 |
Last Updated: | October 30, 2008 |
ClinicalTrials.gov Identifier: | NCT00783250 |
Health Authority: | Italy: National Monitoring Centre for Clinical Trials - Ministry of Health |
COPD Respiratory Mechanics Bronchodilators COPD patients with poor reversibility |
Lung Diseases, Obstructive Respiratory Tract Diseases Lung Diseases |
Albuterol Tiotropium Pulmonary Disease, Chronic Obstructive |
Parasympatholytics Respiratory System Agents Neurotransmitter Agents Cholinergic Antagonists Molecular Mechanisms of Pharmacological Action Adrenergic beta-Agonists Adrenergic Agents Physiological Effects of Drugs Anti-Asthmatic Agents |
Reproductive Control Agents Cholinergic Agents Pharmacologic Actions Adrenergic Agonists Tocolytic Agents Autonomic Agents Therapeutic Uses Peripheral Nervous System Agents Bronchodilator Agents |