ID
16223
Beschrijving
Fulvestrant in Premenopausal Women With Hormone Receptor-Positive Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00146601
Link
https://clinicaltrials.gov/show/NCT00146601
Trefwoorden
Versies (1)
- 06-07-16 06-07-16 -
Geüploaded op
6 juli 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00146601
Eligibility Breast Cancer NCT00146601
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Hormone Therapy Metastatic Neoplasm
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0279025
- UMLS CUI [1,2]
- C2939420
Beschrijving
Pregnancy | Breast Feeding
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Beschrijving
Postmenopausal state
Datatype
boolean
Alias
- UMLS CUI [1]
- C0232970
Beschrijving
Hormone Therapy | Chemotherapy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0279025
- UMLS CUI [2]
- C0392920
Beschrijving
fulvestrant
Datatype
boolean
Alias
- UMLS CUI [1]
- C0935916
Beschrijving
Chemotherapy Regimen Metastatic Neoplasm
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0392920
- UMLS CUI [1,2]
- C2939420
Beschrijving
Anticoagulation Therapy Long-term
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003281
- UMLS CUI [1,2]
- C0443252
Beschrijving
Intercurrent disease Severe Uncontrolled
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0277557
- UMLS CUI [1,2]
- C0205082
- UMLS CUI [1,3]
- C0205318
Beschrijving
Hypersensitivity Castor Oil
Datatype
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])