ID

14185

Description

Methods of Determining Asthma Severity in Children; ODM derived from: https://clinicaltrials.gov/show/NCT00132834

Lien

https://clinicaltrials.gov/show/NCT00132834

Mots-clés

  1. 04/04/2016 04/04/2016 -
Détendeur de droits

CC BY-NC 3.0

Téléchargé le

4 avril 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Asthma NCT00132834

Eligibility Asthma NCT00132834

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00132834
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
physician-diagnosed asthma
Description

asthma

Type de données

boolean

Alias
UMLS CUI [1]
C0004096
symptoms consistent with persistent asthma in the year prior to study entry
Description

persistent asthma

Type de données

boolean

Alias
UMLS CUI [1,1]
C3266628
UMLS CUI [1,2]
C0040223
able to speak and understand english
Description

english

Type de données

boolean

Alias
UMLS CUI [1]
C0376245
parent or guardian willing to provide informed consent
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0030551
Exclusion criteria
Description

Exclusion criteria

Alias
UMLS CUI-1
C0680251
diagnoses indicating other lung-related disorders (e.g., cystic fibrosis, bronchopulmonary dysplasia [bpd])
Description

lung disease

Type de données

boolean

Alias
UMLS CUI [1]
C0024115
allergy to latex
Description

allergy to latex

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0023115
smoker
Description

smoker

Type de données

boolean

Alias
UMLS CUI [1]
C0543414
albuterol use within 12 hours of study entry
Description

albuterol

Type de données

boolean

Alias
UMLS CUI [1,1]
C0001927
UMLS CUI [1,2]
C0040223
long-acting bronchodilator or leukotriene modifier use within 24 hours of study entry
Description

long-acting bronchodilator or leukotriene modifier

Type de données

boolean

Alias
UMLS CUI [1,1]
C2936789
UMLS CUI [1,2]
C0040223
unable to use the r-tube. more information on this criterion can be found in the dait icac-ebc protocol.
Description

r-tube

Type de données

boolean

exclusion criteria for part a participants: ics or oral corticosteroid use in the month prior to study entry
Description

ics or oral corticosteroid use

Type de données

boolean

Alias
UMLS CUI [1,1]
C3248292
UMLS CUI [1,2]
C0040223
UMLS CUI [2,1]
C3653473
UMLS CUI [2,2]
C0040223

Similar models

Eligibility Asthma NCT00132834

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00132834
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
asthma
Item
physician-diagnosed asthma
boolean
C0004096 (UMLS CUI [1])
persistent asthma
Item
symptoms consistent with persistent asthma in the year prior to study entry
boolean
C3266628 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
english
Item
able to speak and understand english
boolean
C0376245 (UMLS CUI [1])
informed consent
Item
parent or guardian willing to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0030551 (UMLS CUI [1,2])
Item Group
Exclusion criteria
C0680251 (UMLS CUI-1)
lung disease
Item
diagnoses indicating other lung-related disorders (e.g., cystic fibrosis, bronchopulmonary dysplasia [bpd])
boolean
C0024115 (UMLS CUI [1])
allergy to latex
Item
allergy to latex
boolean
C0020517 (UMLS CUI [1,1])
C0023115 (UMLS CUI [1,2])
smoker
Item
smoker
boolean
C0543414 (UMLS CUI [1])
albuterol
Item
albuterol use within 12 hours of study entry
boolean
C0001927 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
long-acting bronchodilator or leukotriene modifier
Item
long-acting bronchodilator or leukotriene modifier use within 24 hours of study entry
boolean
C2936789 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
r-tube
Item
unable to use the r-tube. more information on this criterion can be found in the dait icac-ebc protocol.
boolean
ics or oral corticosteroid use
Item
exclusion criteria for part a participants: ics or oral corticosteroid use in the month prior to study entry
boolean
C3248292 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C3653473 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial