ID

34179

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02334709

Nyckelord

  1. 2019-01-15 2019-01-15 -
Rättsinnehavare

GSK group of companies

Uppladdad den

15 januari 2019

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Carcinoma, Renal Cell NCT02334709

Eligibility Carcinoma, Renal Cell NCT02334709

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent
Beskrivning

ID.1

Datatyp

boolean

diagnosis of rcc with clear-cell component histology
Beskrivning

ID.2

Datatyp

boolean

at least 3 extracranial measurable metastatic lesions per recist
Beskrivning

ID.3

Datatyp

boolean

karnofsky performance score >60
Beskrivning

ID.4

Datatyp

boolean

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

ID.5

Datatyp

boolean

patients should have adequate organ function for tki treatment.
Beskrivning

ID.6

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior systemic treatment for rcc
Beskrivning

ID.7

Datatyp

boolean

uncontrolled central nervous metastases
Beskrivning

ID.8

Datatyp

boolean

prior radiotherapy interfering with sbrt
Beskrivning

ID.9

Datatyp

boolean

any disorder precluding understanding of trial information.
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Carcinoma, Renal Cell NCT02334709

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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