ID
13578
Beschrijving
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
Trefwoorden
Versies (1)
- 17-02-16 17-02-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
17 februari 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Acute Myeloid Leukemia NCT00150878
Eligibility Acute Myeloid Leukemia NCT00150878
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
aml with t(5;17)
Datatype
boolean
Alias
- UMLS CUI [1]
- C0023467
Beschrijving
aml with t((8;21)
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0023467
- UMLS CUI [1,2]
- C3897139
Beschrijving
clinically relevant heart failure (nyha ii-iv)
Datatype
boolean
Alias
- UMLS CUI [1]
- C1275491
Beschrijving
renal failure (creatinine > 200 µg/ml)
Datatype
boolean
Alias
- UMLS CUI [1]
- C0201976
Beschrijving
liver function failure (bilirubin > 3 mg/dl)
Datatype
boolean
Alias
- UMLS CUI [1]
- C1278039
Beschrijving
concomitant neurological or psychiatric disease
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
Beschrijving
contraindications to receive prescribed study medication
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C0013227
Beschrijving
hiv infection
Datatype
boolean
Alias
- UMLS CUI [1]
- C0019693
Beschrijving
pregnancy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
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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])