Informations:
Erreur:
ID
22870
Description
Stop Emergency Room Visits for Hyperglycemia Project - District of Columbia (DC); ODM derived from: https://clinicaltrials.gov/show/NCT01033773
Lien
https://clinicaltrials.gov/show/NCT01033773
Mots-clés
Versions (1)
- 13/06/17 13/06/17 -
Téléchargé le
13 giugno 2017
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility Type 2 Diabetes Mellitus NCT01033773
Eligibility Type 2 Diabetes Mellitus NCT01033773
- StudyEvent: Eligibility
Similar models
Eligibility Type 2 Diabetes Mellitus NCT01033773
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
type 2 diabetes mellitus
Item
type 2 diabetes mellitus,
boolean
C0011860 (UMLS CUI [1])
random bg
Item
random bg > 200 mg/dl,
boolean
C0428567 (UMLS CUI [1])
informed consent, diabetes self-management education
Item
willing and able to provide informed consent and to participate in diabetes self-management education (dsme)
boolean
C0021430 (UMLS CUI [1])
C3698325 (UMLS CUI [2])
C3698325 (UMLS CUI [2])
stable for discharge from the ed once hyperglycemia treatment initiated
Item
stable for discharge from the ed once hyperglycemia treatment initiated.
boolean
C0150252 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0030685 (UMLS CUI [1,3])
C0205360 (UMLS CUI [1,2])
C0030685 (UMLS CUI [1,3])
type 1 diabetes mellitus
Item
type 1 diabetes mellitus,
boolean
C0011854 (UMLS CUI [1])
diabetic ketoacidosis or hyperosmolar non-ketotic state
Item
diabetic ketoacidosis or hyperosmolar non-ketotic state,
boolean
C0011880 (UMLS CUI [1])
C0553772 (UMLS CUI [2])
C0553772 (UMLS CUI [2])
concomitant treatment with glucocorticoids
Item
concomitant treatment with glucocorticoids (other than stable maintenance dose therapy),
boolean
C0149783 (UMLS CUI [1])
cognitive or physical impairment
Item
cognitive or physical impairment preventing participation in dsme
boolean
C0338656 (UMLS CUI [1])
C0231171 (UMLS CUI [2])
C0231171 (UMLS CUI [2])
informed consent, compliance
Item
unwillingness or inability to provide consent and/or attend follow-up visits.
boolean
C0021430 (UMLS CUI [1])
C1321605 (UMLS CUI [2])
C1321605 (UMLS CUI [2])