ID
4404
Description
ODM derived from http://clinicaltrials.gov/show/NCT00857012
Link
http://clinicaltrials.gov/show/NCT00857012
Keywords
Versions (2)
- 12/9/13 12/9/13 - Martin Dugas
- 12/16/14 12/16/14 - Martin Dugas
Uploaded on
December 9, 2013
DOI
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License
Creative Commons BY-NC 3.0 Legacy
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Eligibility NCT00857012 Breast Cancer
Eligibility
- StudyEvent: Eligibility
Description
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Description
Patients with severe renal function disorders (Creatinine clearance < 20 ml/min or Patients with moderate or severe disorders of hepatic function
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205082
- SNOMED CT 2011_0131
- 24484000
- UMLS CUI 2011AA
- C1848822
- UMLS CUI 2011AA
- C0373595
- SNOMED CT 2011_0131
- 167181009
- MedDRA 14.1
- 10011371
- UMLS CUI 2011AA
- C1299393
- SNOMED CT 2011_0131
- 371924009
- UMLS CUI 2011AA
- C0086565
- SNOMED CT 2011_0131
- 75183008
- MedDRA 14.1
- 10019670
Description
Concomitant treatment with drugs known to affect sex hormonal status and tamoxifen
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1707479
- UMLS CUI 2011AA
- C0013227
- UMLS CUI 2011AA
- C0392760
- SNOMED CT 2011_0131
- 247591002
- UMLS CUI 2011AA
- C0036884
- SNOMED CT 2011_0131
- 312263009
- UMLS CUI 2011AA
- C0449438
- SNOMED CT 2011_0131
- 263490005
- LOINC Version 232
- MTHU015827
- UMLS CUI 2011AA
- C0039286
- SNOMED CT 2011_0131
- 373345002
- LOINC Version 232
- MTHU003102
Description
Patients with ductal carcinoma in situ (DCIS) without primary diagnosis of early breast cancer (M0)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0007124
- SNOMED CT 2011_0131
- 86616005
- MedDRA 14.1
- 10013806
- ICD-10-CM Version 2010
- D05.1
- UMLS CUI 2011AA
- C0332197
- SNOMED CT 2011_0131
- 2667000
- UMLS CUI 2011AA
- C0801658
- LOINC Version 232
- 18630-4
- UMLS CUI 2011AA
- C1279919
- SNOMED CT 2011_0131
- 264499004
- UMLS CUI 2011AA
- C0678222
- SNOMED CT 2011_0131
- 254838004
- MedDRA 14.1
- 10006204
- UMLS CUI 2011AA
- C0445034
- SNOMED CT 2011_0131
- 30893008
Description
Evidence of any significant clinical disorder or laboratory finding which in the opinion of the investigator, makes it undesirable for the patient to participate in the program
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0332120
- SNOMED CT 2011_0131
- 18669006
- UMLS CUI 2011AA
- C0750502
- SNOMED CT 2011_0131
- 386134007
- UMLS CUI 2011AA
- C0205210
- SNOMED CT 2011_0131
- 58147004
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
- UMLS CUI 2011AA
- C0587081
- SNOMED CT 2011_0131
- 118246004
- UMLS CUI 2011AA
- C0030705
- SNOMED CT 2011_0131
- 116154003
- UMLS CUI 2011AA
- C1548788
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C1709697
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