ID

34148

Description

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

Lien

https://clinicaltrials.gov/show/NCT00723398

Mots-clés

  1. 14/01/2019 14/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

14 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00723398

Eligibility Breast Cancer NCT00723398

Inclusion Criteria
Description

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
Description

ID.1

Type de données

boolean

breast density greater than 25%
Description

ID.2

Type de données

boolean

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

ID.3

Type de données

boolean

non-smokers.
Description

ID.4

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.5

Type de données

boolean

history of atherosclerotic heart disease
Description

ID.6

Type de données

boolean

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

ID.7

Type de données

boolean

diabetes mellitus
Description

ID.8

Type de données

boolean

uncontrolled hypertension (bp ≥140/90)
Description

ID.9

Type de données

boolean

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

ID.10

Type de données

boolean

Similar models

Eligibility Breast Cancer NCT00723398

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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