ID
17236
Description
Letrozole in Postmenopausal Women at Increased Risk for Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00280930
Lien
https://clinicaltrials.gov/show/NCT00280930
Mots-clés
Versions (1)
- 01/09/2016 01/09/2016 -
Téléchargé le
1 septembre 2016
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Post-Menopausal NCT00280930
Eligibility Post-Menopausal NCT00280930
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Mammogram suspicious for breast cancer
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1277190
- UMLS CUI [1,2]
- C0024671
Description
Malignancies, metastatic disease
Type de données
boolean
Alias
- UMLS CUI [1]
- C0006826
- UMLS CUI [2]
- C0027627
Description
uncontrolled metabolic or endocrine disease, cardiovascular disease or malabsorption syndrome
Type de données
boolean
Alias
- UMLS CUI [1]
- C0025517
- UMLS CUI [2]
- C0014130
- UMLS CUI [3]
- C0007222
- UMLS CUI [4]
- C0024523
Description
chemotherapy or immunotherapy
Type de données
boolean
Alias
- UMLS CUI [1]
- C0392920
- UMLS CUI [2]
- C0021083
Description
Hormone replacement therapy or evista (raloxifene)
Type de données
boolean
Alias
- UMLS CUI [1]
- C0282402
- UMLS CUI [2]
- C0618111
Description
Tamoxifen
Type de données
boolean
Alias
- UMLS CUI [1]
- C0039286
Similar models
Eligibility Post-Menopausal NCT00280930
- StudyEvent: Eligibility
C0025344 (UMLS CUI [2])
C0202022 (UMLS CUI [3])
C0278321 (UMLS CUI [4])
C1521996 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2])
C0024671 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2])
C0014130 (UMLS CUI [2])
C0007222 (UMLS CUI [3])
C0024523 (UMLS CUI [4])
C0021083 (UMLS CUI [2])
C0618111 (UMLS CUI [2])
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