ID

42958

Beskrivning

Nyckelord

Versioner (4)
  1. 2011-11-11 2011-11-11 -
  2. 2011-11-11 2011-11-11 -
  3. 2014-03-21 2014-03-21 - Martin Dugas
  4. 2021-09-17 2021-09-17 -
Uppladdad den

17 september 2021

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0 Legacy
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Criteria NCT00044564

Engelsk

Eligibility

1 Formulär  
  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion criteria
Beskrivning

Inclusion criteria

Alias
UMLS CUI
C1512693
measurable disease as defined by the presence of at least one measurable lesion
Beskrivning

Advanced Renal Cell Carcinoma

Datatyp

boolean

Alias
UMLS CUI-1
C0007134
prior immunotherapy (up to 2 regimens) or prior radiotherapy is permitted but at least 4 weeks must have elapsed prior to enter study
Beskrivning

Prior immunotherapy or radiotherapy

Datatyp

boolean

Alias
UMLS CUI-1
C0021083
UMLS CUI-2
C1522449
life expectancy of at least 12 weeks
Beskrivning

Life expectancy

Datatyp

boolean

Alias
UMLS CUI-1
C0023671
adequate bone marrow, liver and kidney function
Beskrivning

Bone marrow, liver, kidney

Datatyp

boolean

Alias
UMLS CUI-1
C0023508
UMLS CUI-2
C1287267
UMLS CUI-3
C0019046
UMLS CUI-4
C0525032
UMLS CUI-5
C0011221
UMLS CUI-6
C0010294
Exclusion criteria
Beskrivning

Exclusion criteria

Alias
UMLS CUI
C0680251
excluded medical conditions like: pre-existing neuropathy, active heart diseases or ischemia, serious infections, HIV infection, chronic hepatitis B or C, brain metastasis, seizures, hypersensitivity to taxanes, organ transplants, some previous cancers
Beskrivning

excluded medical conditions

Datatyp

boolean

Alias
UMLS CUI-1
C0442874
UMLS CUI-2
C0018799
UMLS CUI-3
C0009450
UMLS CUI-4
C0019693
UMLS CUI-5
C0019158
UMLS CUI-6
C0220650
UMLS CUI-7
C0036572
UMLS CUI-8
C0274302
UMLS CUI-9
C0029216
UMLS CUI-10
C0006826
excluded therapies and medications, previous and concomitant such as: anticancer chemotherapy or immunotherapy during the study or within 4 weeks prior to study entry; more than two prior anticancer chemotherapy regimens; radiotherapy during study or within 4 weeks prior to study entry; bone marrow transplant
Beskrivning

excluded therapies and medications

Datatyp

boolean

Alias
UMLS CUI-1
C0392920
UMLS CUI-2
C1963758
UMLS CUI-3
C1522449
UMLS CUI-4
C0005961
others: pregnant or breast-feeding patients; both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial; substance abuse, medical, psychological or social conditions that may interfere with the patient's participation
Beskrivning

other exclusion criteria

Datatyp

boolean

Alias
UMLS CUI-1
C0549206
UMLS CUI-2
C0006147
UMLS CUI-3
C2919192
UMLS CUI-4
C0013146
UMLS CUI-5
C0376405
Tillbaka till toppen

Similar models

Eligibility

1 Formulär
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion criteria
C1512693 (UMLS CUI)
Advanced Renal Cell Carcinoma
Item
measurable disease as defined by the presence of at least one measurable lesion
boolean
C0007134 (UMLS CUI-1)
Prior immunotherapy or radiotherapy
Item
prior immunotherapy (up to 2 regimens) or prior radiotherapy is permitted but at least 4 weeks must have elapsed prior to enter study
boolean
C0021083 (UMLS CUI-1)
C1522449 (UMLS CUI-2)
Life expectancy
Item
life expectancy of at least 12 weeks
boolean
C0023671 (UMLS CUI-1)
Bone marrow, liver, kidney
Item
adequate bone marrow, liver and kidney function
boolean
C0023508 (UMLS CUI-1)
C1287267 (UMLS CUI-2)
C0019046 (UMLS CUI-3)
C0525032 (UMLS CUI-4)
C0011221 (UMLS CUI-5)
C0010294 (UMLS CUI-6)
Item Group
Exclusion criteria
C0680251 (UMLS CUI)
excluded medical conditions
Item
excluded medical conditions like: pre-existing neuropathy, active heart diseases or ischemia, serious infections, HIV infection, chronic hepatitis B or C, brain metastasis, seizures, hypersensitivity to taxanes, organ transplants, some previous cancers
boolean
C0442874 (UMLS CUI-1)
C0018799 (UMLS CUI-2)
C0009450 (UMLS CUI-3)
C0019693 (UMLS CUI-4)
C0019158 (UMLS CUI-5)
C0220650 (UMLS CUI-6)
C0036572 (UMLS CUI-7)
C0274302 (UMLS CUI-8)
C0029216 (UMLS CUI-9)
C0006826 (UMLS CUI-10)
excluded therapies and medications
Item
excluded therapies and medications, previous and concomitant such as: anticancer chemotherapy or immunotherapy during the study or within 4 weeks prior to study entry; more than two prior anticancer chemotherapy regimens; radiotherapy during study or within 4 weeks prior to study entry; bone marrow transplant
boolean
C0392920 (UMLS CUI-1)
C1963758 (UMLS CUI-2)
C1522449 (UMLS CUI-3)
C0005961 (UMLS CUI-4)
other exclusion criteria
Item
others: pregnant or breast-feeding patients; both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial; substance abuse, medical, psychological or social conditions that may interfere with the patient's participation
boolean
C0549206 (UMLS CUI-1)
C0006147 (UMLS CUI-2)
C2919192 (UMLS CUI-3)
C0013146 (UMLS CUI-4)
C0376405 (UMLS CUI-5)
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial