ID

34595

Beschrijving

Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose Monitoring; ODM derived from: https://clinicaltrials.gov/show/NCT01072565

Link

https://clinicaltrials.gov/show/NCT01072565

Trefwoorden

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

see on clinicaltrials.gov

Geüploaded op

19 januari 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Type 2 Diabetes NCT01072565

Eligibility Type 2 Diabetes NCT01072565

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female subjects ≥18 and ≤75 years of age
Beschrijving

ID.1

Datatype

boolean

clinical diagnosis of diabetes
Beschrijving

ID.2

Datatype

boolean

diabetes duration ≥ 1 year
Beschrijving

ID.3

Datatype

boolean

hba1c ≥7.2%
Beschrijving

ID.4

Datatype

boolean

diabetes can be treated with any therapy including medical nutrition therapy alone and any pharmaceutical therapy
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
taken prednisone or cortisone medications in the previous 30 days
Beschrijving

ID.6

Datatype

boolean

currently pregnant or planning pregnancy during the study period
Beschrijving

ID.7

Datatype

boolean

presence of any severe medical or psychological condition or chronic conditions/infections that in the opinion of the investigator would compromise the subject's safety or successful participation in the study
Beschrijving

ID.8

Datatype

boolean

unable to follow the study protocol
Beschrijving

ID.9

Datatype

boolean

unable to speak, read and write in english
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Type 2 Diabetes NCT01072565

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
male or female subjects ≥18 and ≤75 years of age
boolean
ID.2
Item
clinical diagnosis of diabetes
boolean
ID.3
Item
diabetes duration ≥ 1 year
boolean
ID.4
Item
hba1c ≥7.2%
boolean
ID.5
Item
diabetes can be treated with any therapy including medical nutrition therapy alone and any pharmaceutical therapy
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
taken prednisone or cortisone medications in the previous 30 days
boolean
ID.7
Item
currently pregnant or planning pregnancy during the study period
boolean
ID.8
Item
presence of any severe medical or psychological condition or chronic conditions/infections that in the opinion of the investigator would compromise the subject's safety or successful participation in the study
boolean
ID.9
Item
unable to follow the study protocol
boolean
ID.10
Item
unable to speak, read and write in english
boolean

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

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