ID

22870

Beschrijving

Stop Emergency Room Visits for Hyperglycemia Project - District of Columbia (DC); ODM derived from: https://clinicaltrials.gov/show/NCT01033773

Link

https://clinicaltrials.gov/show/NCT01033773

Trefwoorden

  1. 13-06-17 13-06-17 -
Geüploaded op

13 juni 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes Mellitus NCT01033773

Eligibility Type 2 Diabetes Mellitus NCT01033773

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age > 18 years
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
type 2 diabetes mellitus,
Beschrijving

type 2 diabetes mellitus

Datatype

boolean

Alias
UMLS CUI [1]
C0011860
random bg > 200 mg/dl,
Beschrijving

random bg

Datatype

boolean

Alias
UMLS CUI [1]
C0428567
willing and able to provide informed consent and to participate in diabetes self-management education (dsme)
Beschrijving

informed consent, diabetes self-management education

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C3698325
stable for discharge from the ed once hyperglycemia treatment initiated.
Beschrijving

stable for discharge from the ed once hyperglycemia treatment initiated

Datatype

boolean

Alias
UMLS CUI [1,1]
C0150252
UMLS CUI [1,2]
C0205360
UMLS CUI [1,3]
C0030685
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
type 1 diabetes mellitus,
Beschrijving

type 1 diabetes mellitus

Datatype

boolean

Alias
UMLS CUI [1]
C0011854
diabetic ketoacidosis or hyperosmolar non-ketotic state,
Beschrijving

diabetic ketoacidosis or hyperosmolar non-ketotic state

Datatype

boolean

Alias
UMLS CUI [1]
C0011880
UMLS CUI [2]
C0553772
concomitant treatment with glucocorticoids (other than stable maintenance dose therapy),
Beschrijving

concomitant treatment with glucocorticoids

Datatype

boolean

Alias
UMLS CUI [1]
C0149783
cognitive or physical impairment preventing participation in dsme
Beschrijving

cognitive or physical impairment

Datatype

boolean

Alias
UMLS CUI [1]
C0338656
UMLS CUI [2]
C0231171
unwillingness or inability to provide consent and/or attend follow-up visits.
Beschrijving

informed consent, compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C1321605

Similar models

Eligibility Type 2 Diabetes Mellitus NCT01033773

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
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])
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])

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