ID

34276

Descrição

Early Dietary Intervention and Later Signs of Beta-Cell Autoimmunity; ODM derived from: https://clinicaltrials.gov/show/NCT01735123

Link

https://clinicaltrials.gov/show/NCT01735123

Palavras-chave

  1. 16/01/2019 16/01/2019 -
Titular dos direitos

see on clinicaltrials.gov

Transferido a

16 de janeiro de 2019

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 1 NCT01735123

Eligibility Diabetes Mellitus, Type 1 NCT01735123

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
the infant's parents give signed consent to participate and their hla genotype is eligible.
Descrição

ID.1

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
an older sibling of the newborn infant has been included in this study;
Descrição

ID.2

Tipo de dados

boolean

multiple gestation;
Descrição

ID.3

Tipo de dados

boolean

the parents are unwilling or unable to feed the infant cow's milk based products for any reason (e.g., religious, cultural);
Descrição

ID.4

Tipo de dados

boolean

the gestational age of the newborn infant is less than 35 weeks
Descrição

ID.5

Tipo de dados

boolean

inability of the family to take part in the study (e.g. the family had no access to the study center or telephone)
Descrição

ID.6

Tipo de dados

boolean

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.;
Descrição

ID.7

Tipo de dados

boolean

the infant receives any infant formula other than study formula or nutramigen at the delivery hospital
Descrição

ID.8

Tipo de dados

boolean

no hla sample has been drawn before the age of 8 days.
Descrição

ID.9

Tipo de dados

boolean

Similar models

Eligibility Diabetes Mellitus, Type 1 NCT01735123

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
the infant's parents give signed consent to participate and their hla genotype is eligible.
boolean
Item Group
C0680251 (UMLS CUI)
ID.2
Item
an older sibling of the newborn infant has been included in this study;
boolean
ID.3
Item
multiple gestation;
boolean
ID.4
Item
the parents are unwilling or unable to feed the infant cow's milk based products for any reason (e.g., religious, cultural);
boolean
ID.5
Item
the gestational age of the newborn infant is less than 35 weeks
boolean
ID.6
Item
inability of the family to take part in the study (e.g. the family had no access to the study center or telephone)
boolean
ID.7
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
ID.8
Item
the infant receives any infant formula other than study formula or nutramigen at the delivery hospital
boolean
ID.9
Item
no hla sample has been drawn before the age of 8 days.
boolean

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