Informatie:
Fout:
ID
12936
Beschrijving
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
Trefwoorden
Versies (1)
- 06-01-16 06-01-16 -
Geüploaded op
6 januari 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00005605
Eligibility Breast Cancer NCT00005605
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00005605
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
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])