ID

13118

Description

Immunotherapy With APC8015 (Sipuleucel-T, Provenge) for Asymptomatic, Metastatic, Hormone-Refractory Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01133704

Link

https://clinicaltrials.gov/show/NCT01133704

Keywords

  1. 1/17/16 1/17/16 -
Uploaded on

January 17, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Hormone-Refractory Prostate Cancer NCT01133704

Eligibility Hormone-Refractory Prostate Cancer NCT01133704

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically documented adenocarcinoma of the prostate
Description

prostate adenocarcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C0019638
UMLS CUI [1,2]
C0007112
metastatic disease as evidenced by soft tissue and/or bony metastases
Description

metastasis

Data type

boolean

Alias
UMLS CUI [1]
C0027627
prostate-specific antigen value of at least 5 ng/ml
Description

psa

Data type

boolean

Alias
UMLS CUI [1]
C0138741
tumor progression while on hormonal therapy
Description

tumor progression while on hormone therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0178874
UMLS CUI [1,2]
C0279025
castration levels of testosterone (defined as less than 50 ng/dl)
Description

testosterone

Data type

boolean

Alias
UMLS CUI [1]
C0523912
life expectancy of at least 16 weeks
Description

life expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
adequate hematologic, renal, and liver function
Description

organ function

Data type

boolean

Alias
UMLS CUI [1,1]
C0232741
UMLS CUI [1,2]
C0005953
UMLS CUI [1,3]
C0232804
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
visceral organ metastases
Description

visceral metastases

Data type

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0442045
metastatic disease expected to be in need of radiation therapy within 4 months.
Description

radiation therapy

Data type

boolean

Alias
UMLS CUI [1]
C1522449
concurrent therapy with experimental agents
Description

study subject participation status, concurrent therapy

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0009429

Similar models

Eligibility Hormone-Refractory Prostate Cancer NCT01133704

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
prostate adenocarcinoma
Item
histologically documented adenocarcinoma of the prostate
boolean
C0019638 (UMLS CUI [1,1])
C0007112 (UMLS CUI [1,2])
metastasis
Item
metastatic disease as evidenced by soft tissue and/or bony metastases
boolean
C0027627 (UMLS CUI [1])
psa
Item
prostate-specific antigen value of at least 5 ng/ml
boolean
C0138741 (UMLS CUI [1])
tumor progression while on hormone therapy
Item
tumor progression while on hormonal therapy
boolean
C0178874 (UMLS CUI [1,1])
C0279025 (UMLS CUI [1,2])
testosterone
Item
castration levels of testosterone (defined as less than 50 ng/dl)
boolean
C0523912 (UMLS CUI [1])
life expectancy
Item
life expectancy of at least 16 weeks
boolean
C0023671 (UMLS CUI [1])
organ function
Item
adequate hematologic, renal, and liver function
boolean
C0232741 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
C0232804 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
visceral metastases
Item
visceral organ metastases
boolean
C0027627 (UMLS CUI [1,1])
C0442045 (UMLS CUI [1,2])
radiation therapy
Item
metastatic disease expected to be in need of radiation therapy within 4 months.
boolean
C1522449 (UMLS CUI [1])
study subject participation status, concurrent therapy
Item
concurrent therapy with experimental agents
boolean
C2348568 (UMLS CUI [1])
C0009429 (UMLS CUI [2])

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