ID
13706
Beskrivning
Everolimus (RAD001) in Elderly Patients With Acute Myeloid Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00636922
Länk
https://clinicaltrials.gov/show/NCT00636922
Nyckelord
Versioner (1)
- 2016-02-29 2016-02-29 -
Rättsinnehavare
CC BY-NC 3.0
Uppladdad den
29 februari 2016
DOI
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Licens
Creative Commons BY-NC 3.0
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Eligibility Acute Myeloid Leukemia NCT00636922
Eligibility Acute Myeloid Leukemia NCT00636922
- StudyEvent: Eligibility
Beskrivning
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beskrivning
any serious medical or psychiatric conditions which the investigator feels may interfere with the patient's ability to give informed consent or participate in the procedures or evaluations of the study
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Beskrivning
history of major non-compliance to medication
Datatyp
boolean
Alias
- UMLS CUI [1]
- C1321605
Beskrivning
evidence of cns leukemia
Datatyp
boolean
Alias
- UMLS CUI [1]
- C1332884
Beskrivning
uncontrolled viral infection with known hiv or hepatitis type b or c
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0019682
- UMLS CUI [2]
- C0019163
- UMLS CUI [3]
- C0019196
Beskrivning
currently active gastrointestinal disease (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhoea, malabsorption syndrome, or small bowel resection), or other disease, that prevents the patient from absorbing or taking oral medication
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0009488
Beskrivning
any other concurrent severe and/or uncontrolled medical conditions (eg. acute or chronic liver disease, infection, pulmonary disease) that in the opinion of the investigator could potentiate unacceptable safety risks or jeopardize compliance with the protocol
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Beskrivning
males with a female partner of childbearing potential do not agree to use at least 2 effective contraceptive methods throughout the study and for 6 months following the date of last dose
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0700589
Similar models
Eligibility Acute Myeloid Leukemia NCT00636922
- StudyEvent: Eligibility
C0541315 (UMLS CUI [2])
C0201836 (UMLS CUI [2])
C0201899 (UMLS CUI [3])
C0017654 (UMLS CUI [2])
C1272693 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0019163 (UMLS CUI [2])
C0019196 (UMLS CUI [3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])