ID

34596

Beschrijving

Cohort Study in Type 2 Diabetes in China; ODM derived from: https://clinicaltrials.gov/show/NCT01076023

Link

https://clinicaltrials.gov/show/NCT01076023

Trefwoorden

  1. 19-01-19 19-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

19 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes NCT01076023

Eligibility Type 2 Diabetes NCT01076023

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who are 40 years of age or older
Beschrijving

ID.1

Datatype

boolean

patients with confirmed diagnosis of type ii diabetes
Beschrijving

ID.2

Datatype

boolean

patients with 3 or more cvd risk factors or with confirmed/history of cad or history of ischemic stroke
Beschrijving

ID.3

Datatype

boolean

patients who have lab data within 30 days of baseline visit
Beschrijving

ID.4

Datatype

boolean

patients who are willing to return for all follow up visits
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who are not willing or not able to return to the same hospital within 12 months after enrollment
Beschrijving

ID.6

Datatype

boolean

patients who have life threatening or terminal disease, or are physically unable to make follow up visits every 6 months after enrollment
Beschrijving

ID.7

Datatype

boolean

patients have severe heart failure (new york heart association [nyha] class 3-4)
Beschrijving

ID.8

Datatype

boolean

patients with severe renal deficiency (creatinine clearance less than 30 ml/min)
Beschrijving

ID.9

Datatype

boolean

patients who are not willing to sign informed consent form
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Type 2 Diabetes NCT01076023

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients who are 40 years of age or older
boolean
ID.2
Item
patients with confirmed diagnosis of type ii diabetes
boolean
ID.3
Item
patients with 3 or more cvd risk factors or with confirmed/history of cad or history of ischemic stroke
boolean
ID.4
Item
patients who have lab data within 30 days of baseline visit
boolean
ID.5
Item
patients who are willing to return for all follow up visits
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
patients who are not willing or not able to return to the same hospital within 12 months after enrollment
boolean
ID.7
Item
patients who have life threatening or terminal disease, or are physically unable to make follow up visits every 6 months after enrollment
boolean
ID.8
Item
patients have severe heart failure (new york heart association [nyha] class 3-4)
boolean
ID.9
Item
patients with severe renal deficiency (creatinine clearance less than 30 ml/min)
boolean
ID.10
Item
patients who are not willing to sign informed consent form
boolean

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