FRESH-PEF175-en
Study of PROXimology in seveRe persistent Asthma
PROXAIR
| Name | Country code |
|---|---|
| France | fr |
['Participant-reported health data']
Individuals
| Topic | Vocabulary |
|---|---|
| Pulmonary medicine | health theme |
| Asthma | cim-11 |
{"level_sex_clusion_I":[{"value":"Male","concept":{"vocab":"MeSH","vocabURI":"D008297"}},{"value":"Female","concept":{"vocab":"MeSH","vocabURI":"D005260"}}],"level_age_clusion_I":[{"value":"Young Adult (19 to 24 years)","concept":{"vocab":"MeSH","vocabURI":"D055815"}},{"value":"Adult (25 to 44 years)","concept":{"vocab":"MeSH","vocabURI":"D000328"}},{"value":"Middle Aged (45 to 64 years)","concept":{"vocab":"MeSH","vocabURI":"D008875"}},{"value":"Aged (65 to 79 years)","concept":{"vocab":"MeSH","vocabURI":"D000368"}}],"level_type_clusion_I":"General population","level_type_clusion_other":"","clusion_I":"Patient inclusion Criteria : - Ambulatory patients, able to cooperate, of either sex, at least 18 years of age. ","clusion_E":"micronized forms in metered-dose inhalers,≥800 µg/d of beclometasone dipropionate in micronized form in metered-dose inhalers or ≥800 µg/j of budesonide or ≥500 µg/d of fluticasone propionate) and of inhaled long-acting ß2 agonists, administered:either in the form of two specialties using one or two of the following inhalers: Aerolizer®, standard metered-dose inhaler, Autohaler, Diskus®, Turbuhaler®,or in the form of a fixed association using one of the following inhalers: standard metered-dose inhaler, Diskus®, Turbuhaler®. - Patients with FEV measurement in the previous month. - Patients who brought their inhaled steroid treatment and inhaled long-acting ß2-agonist at the time of consultation. - Patients in couple whether or not married - Patients and relatives agree to participatePatientCriteria :- Patients with a non-asthmatic OCPD. - Patients who had inhaled steroids or lLABA treatment change in the previous three months (add-on or change of drug, posology change). - Patients and relatives refusing to participate to the study - Parents/ those close unable to complete a self-questionnaire. - Patients who do not live as a couple"}
| Name |
|---|
| Anne;PONTHIEUX |
| Name | Role |
|---|---|
| NOVARTIS PHARMA SAS | sponsor |
| Name |
|---|
| NOVARTIS PHARMA SAS |
| Agency name |
|---|
| CNIL |
['Through independent healthcare practitioners']
['{"concept":{"vocabURI":"Other","vocab":"CESSDA"},"value":"Other"}']
Access on specific project only
Observational Study
| Start | End |
|---|---|
| 2006-01-01 | 2007-01-01 |
One-time cross-sectional study
| Standard |
|---|
| ['GINA classification'] |
{"value":"To be defined","extLink":[]}
| Name | |
|---|---|
| Anne;PONTHIEUX | anne.ponthieux@novartis.com |