ID

34148

Beskrivning

Nutritional Supplements and Hormonal Manipulations for Breast Cancer Prevention; ODM derived from: https://clinicaltrials.gov/show/NCT00723398

Länk

https://clinicaltrials.gov/show/NCT00723398

Nyckelord

  1. 2019-01-14 2019-01-14 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

14 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00723398

Eligibility Breast Cancer NCT00723398

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
postmenopausal status defined as history of at least 12 months without spontaneous menstrual bleeding or a documented hysterectomy and bilateral salpingo oophorectomy
Beskrivning

ID.1

Datatyp

boolean

breast density greater than 25%
Beskrivning

ID.2

Datatyp

boolean

no hormone replacement therapy for at least six months prior to entry into this study
Beskrivning

ID.3

Datatyp

boolean

non-smokers.
Beskrivning

ID.4

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of stroke, pulmonary embolism or deep vein thrombosis
Beskrivning

ID.5

Datatyp

boolean

history of atherosclerotic heart disease
Beskrivning

ID.6

Datatyp

boolean

presence of any known hypercoagulable state either congenital (e.g., protein s deficiency) or acquired (e.g., corticosteroid treatment)
Beskrivning

ID.7

Datatyp

boolean

diabetes mellitus
Beskrivning

ID.8

Datatyp

boolean

uncontrolled hypertension (bp ≥140/90)
Beskrivning

ID.9

Datatyp

boolean

presence of a psychiatric condition that would interfere with adherence to the protocol.
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Breast Cancer NCT00723398

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
postmenopausal status defined as history of at least 12 months without spontaneous menstrual bleeding or a documented hysterectomy and bilateral salpingo oophorectomy
boolean
ID.2
Item
breast density greater than 25%
boolean
ID.3
Item
no hormone replacement therapy for at least six months prior to entry into this study
boolean
ID.4
Item
non-smokers.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
history of stroke, pulmonary embolism or deep vein thrombosis
boolean
ID.6
Item
history of atherosclerotic heart disease
boolean
ID.7
Item
presence of any known hypercoagulable state either congenital (e.g., protein s deficiency) or acquired (e.g., corticosteroid treatment)
boolean
ID.8
Item
diabetes mellitus
boolean
ID.9
Item
uncontrolled hypertension (bp ≥140/90)
boolean
ID.10
Item
presence of a psychiatric condition that would interfere with adherence to the protocol.
boolean

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