ID
46
Beschreibung
Evaluation of Bay 59-8862 in Patients With Advanced Renal Cell Carcinoma Inclusion Criteria: - measurable disease as defined by the presence of at least one measurable lesion - prior immunotherapy (up to 2 regimens) or prior radiotherapy is permitted but at least 4 weeks must have elapsed prior to enter study - life expectancy of at least 12 weeks - adequate bone marrow, liver and kidney function Exclusion Criteria: - excluded medical conditions like: pre-existing neuropathy, active heart diseases or ischemia, serious infections, HIV infection, chronic hepatitis B or C, brain metastasis, seizures, hypersensitivity to taxanes, organ transplants, some previous cancers - excluded therapies and medications, previous and concomitant such as: anticancer chemotherapy or immunotherapy during the study or within 4 weeks prior to study entry; more than two prior anticancer chemotherapy regimens; radiotherapy during study or within 4 weeks prior to study entry; bone marrow transplant - others: pregnant or breast-feeding patients; both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial; substance abuse, medical, psychological or social conditions that may interfere with the patient's participation
Stichworte
Versionen (4)
- 11.11.11 11.11.11 -
- 11.11.11 11.11.11 -
- 21.03.14 21.03.14 - Martin Dugas
- 17.09.21 17.09.21 -
Hochgeladen am
11. November 2011
DOI
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Lizenz
Creative Commons BY-NC 3.0 Legacy
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NCT00044564 Evaluation of Bay 59-8862 in Patients With Advanced Renal Cell Carcinoma
Eligibility
- StudyEvent: Eligibility
Beschreibung
Exclusion criteria
Beschreibung
excluded medical conditions
Datentyp
boolean
Beschreibung
excluded therapies and medications
Datentyp
boolean
Beschreibung
other exclusion criteria
Datentyp
boolean
Beschreibung
Medical concepts
Beschreibung
Diagnosis
Datentyp
string
Alias
- UMLS CUI
- C0011900
- SNOMED CT 2010_0731
- 439401001
Beschreibung
Immunotherapy
Datentyp
string
Alias
- UMLS CUI
- C0021083
- SNOMED CT 2010_0731
- 146638005
Beschreibung
Radiotherapy
Datentyp
string
Alias
- UMLS CUI
- C1522449
- SNOMED CT 2010_0731
- 302505005
Beschreibung
Life expectancy
Datentyp
string
Alias
- UMLS CUI
- C0023671
- LOINC Version 232
- LP75025-4
Beschreibung
WBC
Datentyp
string
Alias
- SNOMED CT 2010_0731
- 767002
- LOINC
- 6690-2
Beschreibung
Platelet count
Datentyp
string
Alias
- SNOMED CT 2010_0731
- 365632008
- UMLS CUI
- C1287267
- LOINC
- 777-3
Beschreibung
Hemoglobin
Datentyp
string
Alias
- SNOMED CT 2010_0731
- 38082009
- UMLS CUI
- C0019046
- MedDRA 13.1
- 10019481
- LOINC
- LP14449-0
Beschreibung
INR
Datentyp
string
Alias
- UMLS CUI
- C0525032
- SNOMED CT 2010_0731
- 165581004
- MedDRA 13.1
- 10022400
- LOINC
- LP20762-8
Beschreibung
Bilirubin
Datentyp
string
Alias
- SNOMED CT 2010_0731
- 79706000
- UMLS CUI
- C0011221
- MedDRA Version 13.1
- 10004683
- LOINC
- 1975-2
Beschreibung
Creatinine
Datentyp
string
Alias
- UMLS CUI
- C0010294
- SNOMED CT 2010_0731
- 15373003
- LOINC
- 38483-4
- MedDRA 13.1
- 10011358
Beschreibung
Neuropathy
Datentyp
string
Alias
- UMLS CUI
- C0442874
- SNOMED CT 2010_0731
- 386033004
- MedDRA 13.1
- 10029328
Beschreibung
Cardiac disease
Datentyp
string
Alias
- UMLS CUI
- C0018799
- SNOMED CT 2010_0731
- 56265001
- MedDRA 13.1
- 10061024
Beschreibung
Infection
Datentyp
string
Alias
- UMLS CUI
- C0021311
- SNOMED CT 2010_0731
- 257551009
- MedDRA Version 13.1
- 10021789
Beschreibung
HIV negative
Datentyp
string
Alias
- UMLS CUI
- C0481430
- SNOMED CT 2010_0731
- 143223008
- MedDRA 13.1
- 10020179
Beschreibung
Hepatitis
Datentyp
string
Alias
- SNOMED CT 2010_0731
- 29001004
- UMLS CUI
- C0019158
- MedDRA Version 13.1
- 10019717
- LOINC
- LP20771-9
Beschreibung
Metastasis
Datentyp
string
Alias
- UMLS CUI
- C0027627
- SNOMED CT 2010_0731
- 128462008
- MedDRA 13.1
- 10027449
- LOINC Version 232
- LP35033-7
Beschreibung
Allergic reaction, due to correct medicinal substance properly administered
Datentyp
string
Alias
- UMLS CUI
- C0274302
- SNOMED CT 2010_0731
- 57302007
Beschreibung
Organ transplant
Datentyp
string
Alias
- UMLS CUI
- C0029216
- MedDRA 13.1
- 10061890
- LOINC Version 232
- MTHU000173
Beschreibung
Pharmaceutical Preparations
Datentyp
string
Alias
- UMLS CUI
- C0013227
Beschreibung
Chemotherapy
Datentyp
string
Alias
- UMLS CUI
- C0392920
- SNOMED CT 2010_0731
- 150415003
Beschreibung
Immunomodulatory or immunosuppressive therapy
Datentyp
string
Alias
- SNOMED CT 2010_0731
- 86553008
- UMLS CUI
- C1963758
- MedDRA Version 13.1
- 10067473
Beschreibung
Radiotherapy
Datentyp
string
Alias
- UMLS CUI
- C1522449
- SNOMED CT 2010_0731
- 302505005
Beschreibung
pregnant
Datentyp
string
Alias
- UMLS CUI
- C0549206
- MedDRA 13.1
- 10036586
Beschreibung
Lactation
Datentyp
string
Alias
- UMLS CUI
- C0006147
- MedDRA 13.1
- 10006247
Beschreibung
Contraception
Datentyp
string
Alias
- UMLS CUI
- C0700589
- SNOMED CT 2010_0731
- 146680009
- MedDRA 13.1
- 10010808
Beschreibung
Drug abuse
Datentyp
string
Alias
- UMLS CUI
- C0013146
- SNOMED CT 2010_0731
- 26416006
- MedDRA 13.1
- 10013654
- LOINC
- LP36310-8
- ICD-9-CM Version 2011
- 305.90
Beschreibung
Compliance
Datentyp
string
Alias
- UMLS CUI
- C1321605
- SNOMED CT 2010_0731
- 405078008
Ähnliche Modelle
Eligibility
- StudyEvent: Eligibility
439401001 (SNOMED CT 2010_0731)
146638005 (SNOMED CT 2010_0731)
302505005 (SNOMED CT 2010_0731)
386033004 (SNOMED CT 2010_0731)
10029328 (MedDRA 13.1)
56265001 (SNOMED CT 2010_0731)
10061024 (MedDRA 13.1)
257551009 (SNOMED CT 2010_0731)
10021789 (MedDRA Version 13.1)
143223008 (SNOMED CT 2010_0731)
10020179 (MedDRA 13.1)
128462008 (SNOMED CT 2010_0731)
10027449 (MedDRA 13.1)
LP35033-7 (LOINC Version 232)
57302007 (SNOMED CT 2010_0731)
150415003 (SNOMED CT 2010_0731)
C1963758 (UMLS CUI)
10067473 (MedDRA Version 13.1)
302505005 (SNOMED CT 2010_0731)
10036586 (MedDRA 13.1)
10006247 (MedDRA 13.1)
146680009 (SNOMED CT 2010_0731)
10010808 (MedDRA 13.1)
26416006 (SNOMED CT 2010_0731)
10013654 (MedDRA 13.1)
LP36310-8 (LOINC)
305.90 (ICD-9-CM Version 2011)
405078008 (SNOMED CT 2010_0731)