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This study will evaluate the correct use of sequential formoterol and budesonide inhaler capsule treatment via Aerolizer and patient satisfaction in adult asthmatics.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Formoterol and Budesonide | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Foradil Combi (Formoterol-budesonide) | Drug |
|
| Measure | Description | Time Frame |
|---|---|---|
| Proper use of Foradil Combi | Day 0, Day 30, Day 90 |
| Measure | Description | Time Frame |
|---|---|---|
| Asthma control test | Day 0, Day 30, Day 90 | |
| Ease of use: FSI-10 Questionnaire | Day 30, Day 90 | |
| Patient Satisfaction: PSAM and FSI-10 |
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Inclusion Criteria:
Exclusion Criteria:
Other protocol-defined inclusion/exclusion criteria may apply.
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| Name | Affiliation | Role |
|---|---|---|
| Novartis Pharmaceuticals | Novartis Pharmaceuticals | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Novartis Investigator Site | Ankara | Turkey (Türkiye) | ||||
| Novarits Investigator Site |
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| Evaluations will be made at visit 2 (Day 30± 1) and 3 (Day 90± 3) |
| Safety: Adverse events and severe adverse events | 3 Months |
| Istanbul |
| Turkey (Türkiye) |
| Novartis Investigator Site | Istanbul | Turkey (Türkiye) |
| Novartis Investigator Site | Izmir | Turkey (Türkiye) |
| ID | Term |
|---|---|
| D001249 | Asthma |
| ID | Term |
|---|---|
| D001982 | Bronchial Diseases |
| D012140 | Respiratory Tract Diseases |
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012130 | Respiratory Hypersensitivity |
| D006969 | Hypersensitivity, Immediate |
| D006967 | Hypersensitivity |
| D007154 | Immune System Diseases |
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