ID

21630

Beschrijving

Comparison Study of Rituximab Plus Sargramostim to Rituximab Alone for Relapsed Follicular B-cell Lymphoma, a Form of Non-Hodgkin's Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00308087

Link

https://clinicaltrials.gov/show/NCT00308087

Trefwoorden

  1. 27-04-17 27-04-17 -
Geüploaded op

27 april 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Lymphoma, Follicular NCT00308087

Eligibility Lymphoma, Follicular NCT00308087

Criteria
Beschrijving

Criteria

relapsed follicular b-cell lymphoma
Beschrijving

Follicular Lymphoma Relapse

Datatype

boolean

Alias
UMLS CUI [1,1]
C0024301
UMLS CUI [1,2]
C0277556
one or more previous therapies for non-hodgkin's
Beschrijving

Therapeutic procedure Quantity Non-Hodgkin Lymphoma

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0024305
at least one measurable tumor by ct scan or mri
Beschrijving

Measurable Disease Quantity X-Ray Computed Tomography | Measurable Disease Quantity Magnetic Resonance Imaging

Datatype

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0040405
UMLS CUI [2,1]
C1513041
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0024485
additional criteria to be determined at screening visit
Beschrijving

Inclusion criteria Additional

Datatype

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1524062
exclusion criteria (abbreviated list):
Beschrijving

Exclusion Criteria

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
rituximab refractory (less than 6 months from last treatment with rituximab to relapse)
Beschrijving

rituximab refractory | rituximab | Relapse

Datatype

boolean

Alias
UMLS CUI [1,1]
C0393022
UMLS CUI [1,2]
C0205269
UMLS CUI [2]
C0393022
UMLS CUI [3]
C0277556
currently receiving treatment for another cancer
Beschrijving

cancer treatment

Datatype

boolean

Alias
UMLS CUI [1]
C0920425
infection currently being treated
Beschrijving

Communicable Disease Treated

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C1522326
active hepatitis b
Beschrijving

Hepatitis B

Datatype

boolean

Alias
UMLS CUI [1]
C0019163
history of hiv infection
Beschrijving

HIV Infection

Datatype

boolean

Alias
UMLS CUI [1]
C0019693
pregnant
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
additional criteria to be determined at screening visit
Beschrijving

Exclusion Criteria Additional

Datatype

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1524062

Similar models

Eligibility Lymphoma, Follicular NCT00308087

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Follicular Lymphoma Relapse
Item
relapsed follicular b-cell lymphoma
boolean
C0024301 (UMLS CUI [1,1])
C0277556 (UMLS CUI [1,2])
Therapeutic procedure Quantity Non-Hodgkin Lymphoma
Item
one or more previous therapies for non-hodgkin's
boolean
C0087111 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0024305 (UMLS CUI [1,3])
Measurable Disease Quantity X-Ray Computed Tomography | Measurable Disease Quantity Magnetic Resonance Imaging
Item
at least one measurable tumor by ct scan or mri
boolean
C1513041 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0040405 (UMLS CUI [1,3])
C1513041 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0024485 (UMLS CUI [2,3])
Inclusion criteria Additional
Item
additional criteria to be determined at screening visit
boolean
C1512693 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
Exclusion Criteria
Item
exclusion criteria (abbreviated list):
boolean
C0680251 (UMLS CUI [1])
rituximab refractory | rituximab | Relapse
Item
rituximab refractory (less than 6 months from last treatment with rituximab to relapse)
boolean
C0393022 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
C0393022 (UMLS CUI [2])
C0277556 (UMLS CUI [3])
cancer treatment
Item
currently receiving treatment for another cancer
boolean
C0920425 (UMLS CUI [1])
Communicable Disease Treated
Item
infection currently being treated
boolean
C0009450 (UMLS CUI [1,1])
C1522326 (UMLS CUI [1,2])
Hepatitis B
Item
active hepatitis b
boolean
C0019163 (UMLS CUI [1])
HIV Infection
Item
history of hiv infection
boolean
C0019693 (UMLS CUI [1])
Pregnancy
Item
pregnant
boolean
C0032961 (UMLS CUI [1])
Exclusion Criteria Additional
Item
additional criteria to be determined at screening visit
boolean
C0680251 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])

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