ID
13578
Description
Standard vs. Reduced-Intensity Conditioning in Patients With Acute Myeloid Leukemia in First Remission; ODM derived from: https://clinicaltrials.gov/show/NCT00150878
Link
https://clinicaltrials.gov/show/NCT00150878
Keywords
Versions (1)
- 2/17/16 2/17/16 -
Copyright Holder
CC BY-NC 3.0
Uploaded on
February 17, 2016
DOI
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License
Creative Commons BY-NC 3.0
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Eligibility Acute Myeloid Leukemia NCT00150878
Eligibility Acute Myeloid Leukemia NCT00150878
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
aml with t(5;17)
Data type
boolean
Alias
- UMLS CUI [1]
- C0023467
Description
aml with t((8;21)
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0023467
- UMLS CUI [1,2]
- C3897139
Description
clinically relevant heart failure (nyha ii-iv)
Data type
boolean
Alias
- UMLS CUI [1]
- C1275491
Description
renal failure (creatinine > 200 µg/ml)
Data type
boolean
Alias
- UMLS CUI [1]
- C0201976
Description
liver function failure (bilirubin > 3 mg/dl)
Data type
boolean
Alias
- UMLS CUI [1]
- C1278039
Description
concomitant neurological or psychiatric disease
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
Description
contraindications to receive prescribed study medication
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C0013227
Description
hiv infection
Data type
boolean
Alias
- UMLS CUI [1]
- C0019693
Description
pregnancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
Similar models
Eligibility Acute Myeloid Leukemia NCT00150878
- StudyEvent: Eligibility
C0205435 (UMLS CUI [1,2])
C0005953 (UMLS CUI [1,2])
C0086930 (UMLS CUI [1,3])
C2348930 (UMLS CUI [1,2])
C0013018 (UMLS CUI [1,2])
C1518999 (UMLS CUI [1,3])
C3897139 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])