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| ID | Type | Description | Link |
|---|---|---|---|
| 95093 FLU9802 NAC-NL-11 |
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| Name | Class |
|---|---|
| Dutch Health Care Insurance Board | OTHER |
| GlaxoSmithKline | INDUSTRY |
| Zambon SpA | INDUSTRY |
| The Netherlands Asthma Foundation |
The aim of this family practice based study is to determine the long-term treatment effects of two drugs that are presumed to modify the course and progression of chronic obstructive pulmonary disease (COPD), oral N-acetylcysteine and inhaled corticosteroids.
Chronic obstructive pulmonary disease (COPD) is a disorder characterised by symptoms and abnormal tests of expiratory flow that do not change markedly over periods of several months observation. COPD includes chronic bronchitis and emphysema. It is not fully clear which medication is the most efficacious in the long-term treatment of COPD. In contrast to asthma, the efficacy and therefore the precise role of inhaled corticosteroids is less clear in the treatment of patients with COPD. The same applies to another (much less investigated) possibility in the treatment of COPD, the anti-oxidant agent N-acetylcysteine. N-acetylcysteine is used as a mucolytic agent in a variety of clinical conditions, such as acute and chronic bronchitis and cystic fibrosis. The aim of this study, which is performed in family practices, is to determine the 3-year treatment effects and cost-effectiveness of oral N-acetylcysteine versus an inhaled corticosteroid (fluticason propionate) in modifying the course and progression of COPD.
Comparisons: N-acetylcysteine (oral, 600 mg o.d.) and fluticason propionate (dry powder inhalation, 500 mcg b.i.d.) are compared with placebo
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| N-acetylcysteine | Drug | |||
| fluticasone propionate | Drug |
| Measure | Description | Time Frame |
|---|---|---|
| exacerbations of COPD, condition-specific quality of life |
| Measure | Description | Time Frame |
|---|---|---|
| lung function decline, respiratory symptoms |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Tjard RJ Schermer, MSc, PhD | Radboud University Nijmegen Medical Centre, Department of Family Medicine | Principal Investigator |
| Chris van Weel, MD, PhD | Radboud University Nijmegen Medical Centre, Department of Family Medicine | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Family Medicine, University of Maastricht | Maastricht | 6200 MD | Netherlands | |||
| Department of Family Medicine, Radboud University Nijmegen Medical Centre |
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| Label | URL |
|---|---|
| Department of General Practice/Family Medicine, Radboud University Nijmegen Medical Centre | View source |
| Netherlands Asthma Foundation | View source |
| GlaxoSmithKline (study sponsor) |
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| ID | Term |
|---|---|
| D029424 | Pulmonary Disease, Chronic Obstructive |
| D008173 | Lung Diseases, Obstructive |
| D029481 | Bronchitis, Chronic |
| ID | Term |
|---|---|
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
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| ID | Term |
|---|---|
| D000111 | Acetylcysteine |
| D000068298 | Fluticasone |
| ID | Term |
|---|---|
| D003545 | Cysteine |
| D000603 | Amino Acids, Sulfur |
| D013457 | Sulfur Compounds |
| D009930 | Organic Chemicals |
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| OTHER |
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| Nijmegen |
| 6500 HB |
| Netherlands |
| Zambon Group Spa (Study Sponsor) | View source |
| D010335 |
| Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D001991 | Bronchitis |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
| D001982 | Bronchial Diseases |
| D000596 |
| Amino Acids |
| D000602 | Amino Acids, Peptides, and Proteins |
| D000730 | Androstadienes |
| D000736 | Androstenes |
| D000731 | Androstanes |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |