Informatie:
Fout:
ID
13020
Beschrijving
Thalidomide Anti-Angiogenesis Therapy of Relapsed or Refractory Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00083694
Link
https://clinicaltrials.gov/show/NCT00083694
Trefwoorden
Versies (1)
- 12-01-16 12-01-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
12 januari 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Leukemia NCT00083694
Eligibility Leukemia NCT00083694
- StudyEvent: Eligibility
Similar models
Eligibility Leukemia NCT00083694
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
leukemia
Item
diagnosis of refractory or relapsed leukemia: acute leukemia, cml, cllm and mds.
boolean
C0023418 (UMLS CUI [1])
informed consent
Item
signed informed consent, including patient agreeing to use safe contraceptive methods during the treatment and for at least 4 months after the treatment is completed
boolean
C0021430 (UMLS CUI [1])
creatinine
Item
serum creatinine < or = 2.5mg/dl
boolean
C0201976 (UMLS CUI [1])
bilirubin
Item
serum bilirubin< or = 2.5mg/dl
boolean
C1278039 (UMLS CUI [1])
pregnancy
Item
negative pregnancy test
boolean
C0032961 (UMLS CUI [1])
age
Item
age 18 years or older
boolean
C0001779 (UMLS CUI [1])
performance status
Item
performance status < or = 3
boolean
C1518965 (UMLS CUI [1])
pregnant or lactating women
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
chemotherapy or radiation
Item
concurrent treatment with cytotoxic chemotherapy, or radiation
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C1522449 (UMLS CUI [2])
seizures, neurotoxicity, or active cns disease
Item
history of seizures, neurotoxicity, or active cns disease
boolean
C0036572 (UMLS CUI [1])
C0235032 (UMLS CUI [2])
C0007682 (UMLS CUI [3])
C0235032 (UMLS CUI [2])
C0007682 (UMLS CUI [3])
infections
Item
serious infections not controlled by antibiotics
boolean
C0009450 (UMLS CUI [1])