Eligibility Multiple Myeloma NCT00083577

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients must have a confirmed diagnosis of previously treated, active multiple myeloma
Description

multiple myeloma

Data type

boolean

Alias
UMLS CUI [1]
C0026764
myeloma protein should be evident from which to evaluate response
Description

myeloma protein

Data type

boolean

Alias
UMLS CUI [1]
C0027015
must be 18 years of age or older. women of childbearing age and fertile men must use a medically acceptable means of birth control while on study and for 6 months thereafter.
Description

age, contraception

Data type

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0700589
patients must sign an informed consent to participate in this study, and be fully aware of the known teratogenic potential of this drug
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
patients must have a total white blood cell count of 2,000 k/microliters. patients may be anemic or thrombocytopenic provided this is felt to be due to extensive marrow involvement with myeloma
Description

white blood cell count

Data type

boolean

Alias
UMLS CUI [1]
C0023508
patients must have adequate liver function as demonstrated by a direct bilirubin of < or = 2.0 mg/dl.
Description

liver function

Data type

boolean

Alias
UMLS CUI [1]
C1278039
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients must not have an active infection requiring parenteral antibiotics
Description

active infection

Data type

boolean

Alias
UMLS CUI [1]
C0009450
no other concurrent therapy for myeloma is permitted while on thalidomide
Description

concurrent therapy

Data type

boolean

Alias
UMLS CUI [1]
C0039736

Similar models

Eligibility Multiple Myeloma NCT00083577

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
multiple myeloma
Item
all patients must have a confirmed diagnosis of previously treated, active multiple myeloma
boolean
C0026764 (UMLS CUI [1])
myeloma protein
Item
myeloma protein should be evident from which to evaluate response
boolean
C0027015 (UMLS CUI [1])
age, contraception
Item
must be 18 years of age or older. women of childbearing age and fertile men must use a medically acceptable means of birth control while on study and for 6 months thereafter.
boolean
C0001779 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
informed consent
Item
patients must sign an informed consent to participate in this study, and be fully aware of the known teratogenic potential of this drug
boolean
C0021430 (UMLS CUI [1])
white blood cell count
Item
patients must have a total white blood cell count of 2,000 k/microliters. patients may be anemic or thrombocytopenic provided this is felt to be due to extensive marrow involvement with myeloma
boolean
C0023508 (UMLS CUI [1])
liver function
Item
patients must have adequate liver function as demonstrated by a direct bilirubin of < or = 2.0 mg/dl.
boolean
C1278039 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
active infection
Item
patients must not have an active infection requiring parenteral antibiotics
boolean
C0009450 (UMLS CUI [1])
concurrent therapy
Item
no other concurrent therapy for myeloma is permitted while on thalidomide
boolean
C0039736 (UMLS CUI [1])