Eligibility Solid Tumor NCT00701103

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient has metastatic or locally advanced solid tumor or multiple myeloma
Beskrivning

Metastatic or locally advanced solid tumor or multiple myeloma

Datatyp

boolean

Alias
UMLS CUI [1]
C0027627
UMLS CUI [2]
C0677984
UMLS CUI [3]
C0026764
tumor specimen has igf-1r expression
Beskrivning

IGF-1R

Datatyp

boolean

Alias
UMLS CUI [1]
C4044495
patient agrees to use birth control throughout study
Beskrivning

Contraceptive Methods

Datatyp

boolean

Alias
UMLS CUI [1]
C0700589
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient must not be recovering from antineoplastic therapy in the last 4 weeks
Beskrivning

Recovering from antineoplastic therapy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1709864
UMLS CUI [1,2]
C2346834
patient has participated in a clinical trial in the last 4 weeks
Beskrivning

Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
patient has a history of heart problems such as chf, angina, heart attack or stroke in the last 3 months
Beskrivning

Cardiovascular disorder

Datatyp

boolean

Alias
UMLS CUI [1]
C0007222
patient is taking growth hormone or growth hormone inhibitors
Beskrivning

Growth hormone or growth hormone inhibitors

Datatyp

boolean

Alias
UMLS CUI [1]
C0037663
UMLS CUI [2]
C3812146
if female, patient is pregnant or breastfeeding
Beskrivning

Gynaecological Status

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patient is hiv positive
Beskrivning

HIV Seropositivity

Datatyp

boolean

Alias
UMLS CUI [1]
C0019699
patient has a history of hepatitis b or c
Beskrivning

Hepatitis B or C

Datatyp

boolean

Alias
UMLS CUI [1]
C0019163
UMLS CUI [2]
C0019196

Similar models

Eligibility Solid Tumor NCT00701103

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Metastatic or locally advanced solid tumor or multiple myeloma
Item
patient has metastatic or locally advanced solid tumor or multiple myeloma
boolean
C0027627 (UMLS CUI [1])
C0677984 (UMLS CUI [2])
C0026764 (UMLS CUI [3])
IGF-1R
Item
tumor specimen has igf-1r expression
boolean
C4044495 (UMLS CUI [1])
Contraceptive Methods
Item
patient agrees to use birth control throughout study
boolean
C0700589 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Recovering from antineoplastic therapy
Item
patient must not be recovering from antineoplastic therapy in the last 4 weeks
boolean
C1709864 (UMLS CUI [1,1])
C2346834 (UMLS CUI [1,2])
Subject Participation Status
Item
patient has participated in a clinical trial in the last 4 weeks
boolean
C2348568 (UMLS CUI [1])
Cardiovascular disorder
Item
patient has a history of heart problems such as chf, angina, heart attack or stroke in the last 3 months
boolean
C0007222 (UMLS CUI [1])
Growth hormone or growth hormone inhibitors
Item
patient is taking growth hormone or growth hormone inhibitors
boolean
C0037663 (UMLS CUI [1])
C3812146 (UMLS CUI [2])
Gynaecological Status
Item
if female, patient is pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
HIV Seropositivity
Item
patient is hiv positive
boolean
C0019699 (UMLS CUI [1])
Hepatitis B or C
Item
patient has a history of hepatitis b or c
boolean
C0019163 (UMLS CUI [1])
C0019196 (UMLS CUI [2])