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Information:
Fel:
ID
15611
Beskrivning
TRIGR - Primary Prevention Study for Type 1 Diabetes in Children at Risk; ODM derived from: https://clinicaltrials.gov/show/NCT00179777
Länk
https://clinicaltrials.gov/show/NCT00179777
Nyckelord
Versioner (2)
- 2016-06-05 2016-06-05 -
- 2016-06-10 2016-06-10 - Julian Varghese
Uppladdad den
5 juni 2016
DOI
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Licens
Creative Commons BY-NC 3.0
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Eligibility Diabetes Mellitus, Type 1 NCT00179777
Eligibility Diabetes Mellitus, Type 1 NCT00179777
- StudyEvent: Eligibility
Similar models
Eligibility Diabetes Mellitus, Type 1 NCT00179777
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
type 1 diabetes
Item
biological parent and/or full (not half) sibling of the newborn infant has type 1 diabetes as defined by the world health organization
boolean
C0011854 (UMLS CUI [1])
informed consent
Item
the infant's parent or legal guardians give signed consent to participate
boolean
C0021430 (UMLS CUI [1])
trigr intervention
Item
an older sibling of the newborn infant has been included in the trigr intervention
boolean
C0337511 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,2])
multiple gestation
Item
multiple gestation
boolean
C1403697 (UMLS CUI [1])
unable to feed the infant cows milk
Item
the parents are unwilling or unable to feed the infant cow's milk based products for any reason (e.g., religious, cultural).
boolean
C1321605 (UMLS CUI [1,1])
C0349374 (UMLS CUI [1,2])
C0349374 (UMLS CUI [1,2])
severe illness
Item
the newborn infant has a recognizable severe illness such as those due to chromosomal abnormality, congenital malformation, respiratory failure needing assisted ventilation, enzyme deficiencies, etc.
boolean
C0200867 (UMLS CUI [1])
C0000768 (UMLS CUI [2])
C1145670 (UMLS CUI [3])
C0149676 (UMLS CUI [4])
C0000768 (UMLS CUI [2])
C1145670 (UMLS CUI [3])
C0149676 (UMLS CUI [4])
gestational age
Item
the gestational age of the newborn infant is less than 35 weeks.
boolean
C0017504 (UMLS CUI [1])
age
Item
the infant is older than 7 days at randomization.
boolean
C0001779 (UMLS CUI [1])
inability of the family to take part in the study
Item
inability of the family to take part in the study (e.g. the family has no access to any of the study centers, the family has no telephone).
boolean
C2348568 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,2])
any infant formula
Item
the infant has received any infant formula other than nutramigen prior to randomization.
boolean
C0150589 (UMLS CUI [1])
hla sample drawn
Item
no hla sample drawn before the age of 8 days.
boolean
C0019633 (UMLS CUI [1])