ID

34296

Description

Meta-analyses of Fructose and Cardiometabolic Risk; ODM derived from: https://clinicaltrials.gov/show/NCT01363791

Link

https://clinicaltrials.gov/show/NCT01363791

Keywords

  1. 1/16/19 1/16/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 16, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Dyslipidemia NCT01363791

Eligibility Dyslipidemia NCT01363791

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
trials in humans
Description

ID.1

Data type

boolean

oral fructose intervention
Description

ID.2

Data type

boolean

suitable control (i.e. another carbohydrate source in isocaloric exchange for fructose or a control diet which is compared with the same diet supplemented with excess energy from fructose)
Description

ID.3

Data type

boolean

>= 7-days diet duration
Description

ID.4

Data type

boolean

viable endpoint data
Description

ID.5

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
non-human studies
Description

ID.6

Data type

boolean

iv or parenteral fructose
Description

ID.7

Data type

boolean

high fructose corn syrup or sucrose intervention (except where these are the comparators)
Description

ID.8

Data type

boolean

lack of a suitable control
Description

ID.9

Data type

boolean

< 7-days diet duration.
Description

ID.10

Data type

boolean

no viable endpoint data
Description

ID.11

Data type

boolean

Similar models

Eligibility Dyslipidemia NCT01363791

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
trials in humans
boolean
ID.2
Item
oral fructose intervention
boolean
ID.3
Item
suitable control (i.e. another carbohydrate source in isocaloric exchange for fructose or a control diet which is compared with the same diet supplemented with excess energy from fructose)
boolean
ID.4
Item
>= 7-days diet duration
boolean
ID.5
Item
viable endpoint data
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
non-human studies
boolean
ID.7
Item
iv or parenteral fructose
boolean
ID.8
Item
high fructose corn syrup or sucrose intervention (except where these are the comparators)
boolean
ID.9
Item
lack of a suitable control
boolean
ID.10
Item
< 7-days diet duration.
boolean
ID.11
Item
no viable endpoint data
boolean

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