Informazione:
Errore:
ID
12913
Descrizione
Pediatric Asthma Study Using Stepwise Treatment With Two Food And Drug Administration Approved Asthma Medications; ODM derived from: https://clinicaltrials.gov/show/NCT00158834
collegamento
https://clinicaltrials.gov/show/NCT00158834
Keywords
versioni (1)
- 06/01/16 06/01/16 -
Titolare del copyright
CC BY-NC 3.0
Caricato su
6 gennaio 2016
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 3.0
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Eligibility Asthma NCT00158834
Eligibility Asthma NCT00158834
- StudyEvent: Eligibility
Similar models
Eligibility Asthma NCT00158834
- StudyEvent: Eligibility
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
asthma
Item
children with a documented history of asthma.
boolean
C0004096 (UMLS CUI [1])
inhaled steroids
Item
using inhaled steroids from 100 mcg up to 500 mcg twice daily for at least 1 month before study start.
boolean
C2065041 (UMLS CUI [1])
lung function tests
Item
must be able to perform reproducible lung function tests.
boolean
C0024119 (UMLS CUI [1])
RAST or skin prick test
Item
must have a positive rast or skin prick test.
boolean
C0034554 (UMLS CUI [1])
C0430561 (UMLS CUI [2])
C0430561 (UMLS CUI [2])
Hyperreactivity
Item
during the treatment period, the patient has to be hyperreactive (defined as pd20 methacholine < 150 mcg) and/or have a cumulative symptom score of 14 based on the daily record card filled in during the last 2 weeks of the run-in period.
boolean
C1096470 (UMLS CUI [1])
Infection
Item
history of an acute upper or lower respiratory tract infection, middle ear, or sinus infection 4 weeks prior to visit 1.
boolean
C0009450 (UMLS CUI [1])
respiratory disease
Item
admitted to hospital due to a respiratory disease 4 weeks prior to visit 1.
boolean
C0035204 (UMLS CUI [1])
oral corticosteroids
Item
received oral corticosteroids within 4 weeks prior to visit 1.
boolean
C0001617 (UMLS CUI [1])
disorder that affects growth
Item
existence of any disorder that affects growth.
boolean
C0009488 (UMLS CUI [1])
Comorbidity
Item
clinical or laboratory evidence of a serious systemic disease, or suspected hypersensitivity to corticosteroids, lactose or short/long acting b2-agonists.
boolean
C0009488 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C0001617 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0022949 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C2936789 (UMLS CUI [4,2])
C0020517 (UMLS CUI [2,1])
C0001617 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0022949 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C2936789 (UMLS CUI [4,2])