ID

12936

Descripción

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

Palabras clave

  1. 6/1/16 6/1/16 -
Subido en

6 de enero de 2016

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00005605

Eligibility Breast Cancer NCT00005605

Criteria
Descripción

Criteria

histologically proven stage i or ii breast cancer
Descripción

histology

Tipo de datos

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
Descripción

tamoxifen adjuvant

Tipo de datos

boolean

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

age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
sex: female
Descripción

gender

Tipo de datos

boolean

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

premenopausal

Tipo de datos

boolean

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

pregnancy

Tipo de datos

boolean

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

concurrent therapy

Tipo de datos

boolean

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

chemotherapy

Tipo de datos

boolean

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

endocrine therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0279025

Similar models

Eligibility Breast Cancer NCT00005605

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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