ID

34276

Descripción

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

Link

https://clinicaltrials.gov/show/NCT01735123

Palabras clave

  1. 16/1/19 16/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

16 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 1 NCT01735123

Eligibility Diabetes Mellitus, Type 1 NCT01735123

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.2

Tipo de datos

boolean

multiple gestation;
Descripción

ID.3

Tipo de datos

boolean

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

ID.4

Tipo de datos

boolean

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

ID.5

Tipo de datos

boolean

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

ID.6

Tipo de datos

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.;
Descripción

ID.7

Tipo de datos

boolean

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

ID.8

Tipo de datos

boolean

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

ID.9

Tipo de datos

boolean

Similar models

Eligibility Diabetes Mellitus, Type 1 NCT01735123

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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