ID
16223
Description
Fulvestrant in Premenopausal Women With Hormone Receptor-Positive Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00146601
Link
https://clinicaltrials.gov/show/NCT00146601
Keywords
Versions (1)
- 7/6/16 7/6/16 -
Uploaded on
July 6, 2016
DOI
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License
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00146601
Eligibility Breast Cancer NCT00146601
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Hormone Therapy Metastatic Neoplasm
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0279025
- UMLS CUI [1,2]
- C2939420
Description
Pregnancy | Breast Feeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
Postmenopausal state
Data type
boolean
Alias
- UMLS CUI [1]
- C0232970
Description
Hormone Therapy | Chemotherapy
Data type
boolean
Alias
- UMLS CUI [1]
- C0279025
- UMLS CUI [2]
- C0392920
Description
fulvestrant
Data type
boolean
Alias
- UMLS CUI [1]
- C0935916
Description
Chemotherapy Regimen Metastatic Neoplasm
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0392920
- UMLS CUI [1,2]
- C2939420
Description
Anticoagulation Therapy Long-term
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0003281
- UMLS CUI [1,2]
- C0443252
Description
Intercurrent disease Severe Uncontrolled
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0277557
- UMLS CUI [1,2]
- C0205082
- UMLS CUI [1,3]
- C0205318
Description
Hypersensitivity Castor Oil
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0007343
Similar models
Eligibility Breast Cancer NCT00146601
- StudyEvent: Eligibility
C0441772 (UMLS CUI [2])
C0279759 (UMLS CUI [2])
C0279754 (UMLS CUI [3,1])
C0279759 (UMLS CUI [3,2])
C0677922 (UMLS CUI [2])
C0854638 (UMLS CUI [3,1])
C0677922 (UMLS CUI [3,2])
C2939420 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
C0392920 (UMLS CUI [2])
C2939420 (UMLS CUI [1,2])
C0443252 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
C0205318 (UMLS CUI [1,3])
C0007343 (UMLS CUI [1,2])