ID

15611

Beschrijving

TRIGR - Primary Prevention Study for Type 1 Diabetes in Children at Risk; ODM derived from: https://clinicaltrials.gov/show/NCT00179777

Link

https://clinicaltrials.gov/show/NCT00179777

Trefwoorden

Versies (2)
  1. 05-06-16 05-06-16 -
  2. 10-06-16 10-06-16 - Julian Varghese
Geüploaded op

5 juni 2016

DOI

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Licentie

Creative Commons BY-NC 3.0
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Eligibility Diabetes Mellitus, Type 1 NCT00179777

Engels

Eligibility Diabetes Mellitus, Type 1 NCT00179777

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
biological parent and/or full (not half) sibling of the newborn infant has type 1 diabetes as defined by the world health organization
Beschrijving

type 1 diabetes

Datatype

boolean

Alias
UMLS CUI [1]
C0011854
the infant's parent or legal guardians give signed consent to participate
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
an older sibling of the newborn infant has been included in the trigr intervention
Beschrijving

trigr intervention

Datatype

boolean

Alias
UMLS CUI [1,1]
C0337511
UMLS CUI [1,2]
C2348568
multiple gestation
Beschrijving

multiple gestation

Datatype

boolean

Alias
UMLS CUI [1]
C1403697
the parents are unwilling or unable to feed the infant cow's milk based products for any reason (e.g., religious, cultural).
Beschrijving

unable to feed the infant cows milk

Datatype

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0349374
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.
Beschrijving

severe illness

Datatype

boolean

Alias
UMLS CUI [1]
C0200867
UMLS CUI [2]
C0000768
UMLS CUI [3]
C1145670
UMLS CUI [4]
C0149676
the gestational age of the newborn infant is less than 35 weeks.
Beschrijving

gestational age

Datatype

boolean

Alias
UMLS CUI [1]
C0017504
the infant is older than 7 days at randomization.
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
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).
Beschrijving

inability of the family to take part in the study

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0439801
the infant has received any infant formula other than nutramigen prior to randomization.
Beschrijving

any infant formula

Datatype

boolean

Alias
UMLS CUI [1]
C0150589
no hla sample drawn before the age of 8 days.
Beschrijving

hla sample drawn

Datatype

boolean

Alias
UMLS CUI [1]
C0019633
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Similar models

Eligibility Diabetes Mellitus, Type 1 NCT00179777

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