ID

34179

Beschrijving

Phase I/II Trial of Stereotactic Body Radiotherapy With Concurrent Fixed Dose Tyrosine Kinase Inhibitors in Metastatic Renal Cell Carcinoma: Dose Limiting Toxicity and Abscopal Effect.; ODM derived from: https://clinicaltrials.gov/show/NCT02334709

Link

https://clinicaltrials.gov/show/NCT02334709

Trefwoorden

  1. 15-01-19 15-01-19 -
Houder van rechten

GSK group of companies

Geüploaded op

15 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Carcinoma, Renal Cell NCT02334709

Eligibility Carcinoma, Renal Cell NCT02334709

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent
Beschrijving

ID.1

Datatype

boolean

diagnosis of rcc with clear-cell component histology
Beschrijving

ID.2

Datatype

boolean

at least 3 extracranial measurable metastatic lesions per recist
Beschrijving

ID.3

Datatype

boolean

karnofsky performance score >60
Beschrijving

ID.4

Datatype

boolean

patients should have undergone cytoreductive treatment of their rcc at least 6 weeks prior to inclusion
Beschrijving

ID.5

Datatype

boolean

patients should have adequate organ function for tki treatment.
Beschrijving

ID.6

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior systemic treatment for rcc
Beschrijving

ID.7

Datatype

boolean

uncontrolled central nervous metastases
Beschrijving

ID.8

Datatype

boolean

prior radiotherapy interfering with sbrt
Beschrijving

ID.9

Datatype

boolean

any disorder precluding understanding of trial information.
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Carcinoma, Renal Cell NCT02334709

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
signed informed consent
boolean
ID.2
Item
diagnosis of rcc with clear-cell component histology
boolean
ID.3
Item
at least 3 extracranial measurable metastatic lesions per recist
boolean
ID.4
Item
karnofsky performance score >60
boolean
ID.5
Item
patients should have undergone cytoreductive treatment of their rcc at least 6 weeks prior to inclusion
boolean
ID.6
Item
patients should have adequate organ function for tki treatment.
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
prior systemic treatment for rcc
boolean
ID.8
Item
uncontrolled central nervous metastases
boolean
ID.9
Item
prior radiotherapy interfering with sbrt
boolean
ID.10
Item
any disorder precluding understanding of trial information.
boolean

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