ID

34302

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT00947726

Nyckelord

  1. 2019-01-16 2019-01-16 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

16 januari 2019

DOI

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Licens

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
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
>18 years of age
Beskrivning

ID.1

Datatyp

boolean

non insulin-dependent diabetes
Beskrivning

ID.2

Datatyp

boolean

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

ID.3

Datatyp

boolean

capable of understanding and signing consent form
Beskrivning

ID.4

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of ichthyosis vulgaris
Beskrivning

ID.5

Datatyp

boolean

known hypersensitivity to the topical product used in the study
Beskrivning

ID.6

Datatyp

boolean

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

ID.7

Datatyp

boolean

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

ID.8

Datatyp

boolean

presence of foot ulcer
Beskrivning

ID.9

Datatyp

boolean

evidence of gangrene
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Foot Transepidermal Water Loss in Patients in NIDDM NCT00947726

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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