ID

13020

Description

Thalidomide Anti-Angiogenesis Therapy of Relapsed or Refractory Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00083694

Link

https://clinicaltrials.gov/show/NCT00083694

Keywords

  1. 1/12/16 1/12/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

January 12, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Leukemia NCT00083694

Eligibility Leukemia NCT00083694

  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00083694
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of refractory or relapsed leukemia: acute leukemia, cml, cllm and mds.
Description

leukemia

Data type

boolean

Alias
UMLS CUI [1]
C0023418
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
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
serum creatinine < or = 2.5mg/dl
Description

creatinine

Data type

boolean

Alias
UMLS CUI [1]
C0201976
serum bilirubin< or = 2.5mg/dl
Description

bilirubin

Data type

boolean

Alias
UMLS CUI [1]
C1278039
negative pregnancy test
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
age 18 years or older
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
performance status < or = 3
Description

performance status

Data type

boolean

Alias
UMLS CUI [1]
C1518965
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating women
Description

pregnant or lactating women

Data type

boolean

Alias
UMLS CUI [1]
C0032961
concurrent treatment with cytotoxic chemotherapy, or radiation
Description

chemotherapy or radiation

Data type

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1522449
history of seizures, neurotoxicity, or active cns disease
Description

seizures, neurotoxicity, or active cns disease

Data type

boolean

Alias
UMLS CUI [1]
C0036572
UMLS CUI [2]
C0235032
UMLS CUI [3]
C0007682
serious infections not controlled by antibiotics
Description

infections

Data type

boolean

Alias
UMLS CUI [1]
C0009450

Similar models

Eligibility Leukemia NCT00083694

  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00083694
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
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])
Item Group
C0680251 (UMLS CUI)
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])
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])
infections
Item
serious infections not controlled by antibiotics
boolean
C0009450 (UMLS CUI [1])

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