ID

12936

Description

Tamoxifen to Prevent Bone Loss and Heart Disease in Premenopausal Women Receiving Chemotherapy for Stage I or Stage II Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00005605

Link

https://clinicaltrials.gov/show/NCT00005605

Keywords

Versions (1)
  1. 1/6/16 1/6/16 -
Uploaded on

January 6, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00005605

English

Eligibility Breast Cancer NCT00005605

1 forms  
Criteria
Description

Criteria

histologically proven stage i or ii breast cancer
Description

histology

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0699749
UMLS CUI [2]
C0019638
must be scheduled to receive adjuvant chemotherapy with or without tamoxifen
Description

tamoxifen adjuvant

Data type

boolean

Alias
UMLS CUI [1,1]
C0039286
UMLS CUI [1,2]
C0677850
age: 35 to 50
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
sex: female
Description

gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
menopausal status: premenopausal by follicle-stimulating hormone and estradiol levels
Description

premenopausal

Data type

boolean

Alias
UMLS CUI [1,1]
C0279752
UMLS CUI [1,2]
C0202022
UMLS CUI [2,1]
C0279752
UMLS CUI [2,2]
C0337434
not pregnant
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
prior concurrent therapy:
Description

concurrent therapy

Data type

boolean

Alias
UMLS CUI [1]
C0009429
chemotherapy: see disease characteristics
Description

chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
endocrine therapy: see disease characteristics
Description

endocrine therapy

Data type

boolean

Alias
UMLS CUI [1]
C0279025
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Similar models

Eligibility Breast Cancer NCT00005605

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
histology
Item
histologically proven stage i or ii breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0699749 (UMLS CUI [1,2])
C0019638 (UMLS CUI [2])
tamoxifen adjuvant
Item
must be scheduled to receive adjuvant chemotherapy with or without tamoxifen
boolean
C0039286 (UMLS CUI [1,1])
C0677850 (UMLS CUI [1,2])
age
Item
age: 35 to 50
boolean
C0001779 (UMLS CUI [1])
gender
Item
sex: female
boolean
C0079399 (UMLS CUI [1])
premenopausal
Item
menopausal status: premenopausal by follicle-stimulating hormone and estradiol levels
boolean
C0279752 (UMLS CUI [1,1])
C0202022 (UMLS CUI [1,2])
C0279752 (UMLS CUI [2,1])
C0337434 (UMLS CUI [2,2])
pregnancy
Item
not pregnant
boolean
C0032961 (UMLS CUI [1])
concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
chemotherapy
Item
chemotherapy: see disease characteristics
boolean
C0392920 (UMLS CUI [1])
endocrine therapy
Item
endocrine therapy: see disease characteristics
boolean
C0279025 (UMLS CUI [1])
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