ID

34302

Description

Ceramide Containing Multivesicular Emulsion Application . . .; ODM derived from: https://clinicaltrials.gov/show/NCT00947726

Link

https://clinicaltrials.gov/show/NCT00947726

Keywords

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

see on clinicaltrials.gov

Uploaded on

16 de enero de 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Foot Transepidermal Water Loss in Patients in NIDDM NCT00947726

Eligibility Foot Transepidermal Water Loss in Patients in NIDDM NCT00947726

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
>18 years of age
Description

ID.1

Data type

boolean

non insulin-dependent diabetes
Description

ID.2

Data type

boolean

moderate to severe xerosis of both feet [a score of at least 4 on a scale of 0 (normal) to 8 (deep fissuring)]
Description

ID.3

Data type

boolean

capable of understanding and signing consent form
Description

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of ichthyosis vulgaris
Description

ID.5

Data type

boolean

known hypersensitivity to the topical product used in the study
Description

ID.6

Data type

boolean

previous use of high potency steroids (class i and ii) in past 2 week
Description

ID.7

Data type

boolean

presence of acute skin disease or infection, such as vasculitis or cellulitis
Description

ID.8

Data type

boolean

presence of foot ulcer
Description

ID.9

Data type

boolean

evidence of gangrene
Description

ID.10

Data type

boolean

Similar models

Eligibility Foot Transepidermal Water Loss in Patients in NIDDM NCT00947726

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
>18 years of age
boolean
ID.2
Item
non insulin-dependent diabetes
boolean
ID.3
Item
moderate to severe xerosis of both feet [a score of at least 4 on a scale of 0 (normal) to 8 (deep fissuring)]
boolean
ID.4
Item
capable of understanding and signing consent form
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
history of ichthyosis vulgaris
boolean
ID.6
Item
known hypersensitivity to the topical product used in the study
boolean
ID.7
Item
previous use of high potency steroids (class i and ii) in past 2 week
boolean
ID.8
Item
presence of acute skin disease or infection, such as vasculitis or cellulitis
boolean
ID.9
Item
presence of foot ulcer
boolean
ID.10
Item
evidence of gangrene
boolean

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