ID
13706
Description
Everolimus (RAD001) in Elderly Patients With Acute Myeloid Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00636922
Lien
https://clinicaltrials.gov/show/NCT00636922
Mots-clés
Versions (1)
- 29/02/2016 29/02/2016 -
Détendeur de droits
CC BY-NC 3.0
Téléchargé le
29 février 2016
DOI
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Licence
Creative Commons BY-NC 3.0
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Eligibility Acute Myeloid Leukemia NCT00636922
Eligibility Acute Myeloid Leukemia NCT00636922
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
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
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Description
history of major non-compliance to medication
Type de données
boolean
Alias
- UMLS CUI [1]
- C1321605
Description
evidence of cns leukemia
Type de données
boolean
Alias
- UMLS CUI [1]
- C1332884
Description
uncontrolled viral infection with known hiv or hepatitis type b or c
Type de données
boolean
Alias
- UMLS CUI [1]
- C0019682
- UMLS CUI [2]
- C0019163
- UMLS CUI [3]
- C0019196
Description
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
Type de données
boolean
Alias
- UMLS CUI [1]
- C0009488
Description
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
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Description
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
Type de données
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])