ID
13604
Description
Cytarabine in Combination With Arsenic Trioxide vs. Cytarabine Alone in Elderly Patients With Acute Myeloid Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00513305
Link
https://clinicaltrials.gov/show/NCT00513305
Keywords
Versions (1)
- 2/19/16 2/19/16 -
Copyright Holder
CC BY-NC 3.0
Uploaded on
February 19, 2016
DOI
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License
Creative Commons BY-NC 3.0
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Eligibility Acute Myeloid Leukemia NCT00513305
Eligibility Acute Myeloid Leukemia NCT00513305
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
the patient has had previous cytotoxic chemotherapy for acute myeloid leukemia (aml) or myelodysplastic syndrome (mds).
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0392920
- UMLS CUI [1,2]
- C0205156
Description
previous treatment with low-dose cytarabine is not permitted.
Data type
boolean
Alias
- UMLS CUI [1]
- C0010711
Description
the patient has a qt interval outside of the protocol-specified range.
Data type
boolean
Alias
- UMLS CUI [1]
- C0429028
Description
the patient has laboratory values outside of protocol-specified ranges.
Data type
boolean
Alias
- UMLS CUI [1]
- C0022885
Description
the patient is concurrently treated with cytotoxic therapy, radiation, or investigational agents.
Data type
boolean
Alias
- UMLS CUI [1]
- C0677881
- UMLS CUI [2]
- C0851346
- UMLS CUI [3]
- C1875319
Description
the patient has uncontrolled, severe cardiovascular or pulmonary disease or other uncontrolled medical condition.
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
Description
the patient has known central nervous system involvement with aml.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0023467
- UMLS CUI [1,2]
- C0449389
Similar models
Eligibility Acute Myeloid Leukemia NCT00513305
- StudyEvent: Eligibility
C0205156 (UMLS CUI [1,2])
C0851346 (UMLS CUI [2])
C1875319 (UMLS CUI [3])
C0449389 (UMLS CUI [1,2])