ID

13106

Beschrijving

Safety and Efficacy of Fludarabine and Cyclophosphamide + Rituximab; ODM derived from: https://clinicaltrials.gov/show/NCT00393107

Link

https://clinicaltrials.gov/show/NCT00393107

Trefwoorden

  1. 17-01-16 17-01-16 -
Geüploaded op

17 januari 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Follicular Lymphoma NCT00393107

Eligibility Follicular Lymphoma NCT00393107

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically documented who grade 1-2 ,cd20+,follicular lymphoma
Beschrijving

follicular lymphoma, who grade 1-2 ,cd20+

Datatype

boolean

Alias
UMLS CUI [1,1]
C0024301
UMLS CUI [1,2]
C0919553
UMLS CUI [1,3]
C0054946
relapsed follicular lymphoma
Beschrijving

relapse

Datatype

boolean

Alias
UMLS CUI [1]
C0277556
stage iii or iv disease
Beschrijving

staging

Datatype

boolean

Alias
UMLS CUI [1]
C0699749
stage ii patients are eligible if they present with b symptoms or bulky disease
Beschrijving

stage ii with b symptoms, bulky disease

Datatype

boolean

Alias
UMLS CUI [1]
C0699749
UMLS CUI [2]
C1706867
UMLS CUI [3]
C0555954
to have a need for therapy in the opinion of treating clinician
Beschrijving

therapy indication

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C3146298
measurable disease
Beschrijving

measurable disease

Datatype

boolean

Alias
UMLS CUI [1]
C1513041
expected survival of 6 months or more
Beschrijving

life expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
age 18 to 70 years
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
to have undergone < 3 lines of chemotherapy
Beschrijving

chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C0392920
performance status of 0 to 2
Beschrijving

performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
known hiv infections
Beschrijving

hiv

Datatype

boolean

Alias
UMLS CUI [1]
C0019682
known hepatitis b or c
Beschrijving

hepatitis b or c

Datatype

boolean

Alias
UMLS CUI [1]
C0019163
UMLS CUI [2]
C0019196
cns lymphoma
Beschrijving

cns lymphoma

Datatype

boolean

Alias
UMLS CUI [1]
C0280803
previous malignancies, or cardiac, renal, hepatic, or respiratory failure
Beschrijving

comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
pregnant or lactating women and patients of child bearing potential unless using birth control measures
Beschrijving

pregnancy, lactation, contraception

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0700589

Similar models

Eligibility Follicular Lymphoma NCT00393107

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
follicular lymphoma, who grade 1-2 ,cd20+
Item
histologically documented who grade 1-2 ,cd20+,follicular lymphoma
boolean
C0024301 (UMLS CUI [1,1])
C0919553 (UMLS CUI [1,2])
C0054946 (UMLS CUI [1,3])
relapse
Item
relapsed follicular lymphoma
boolean
C0277556 (UMLS CUI [1])
staging
Item
stage iii or iv disease
boolean
C0699749 (UMLS CUI [1])
stage ii with b symptoms, bulky disease
Item
stage ii patients are eligible if they present with b symptoms or bulky disease
boolean
C0699749 (UMLS CUI [1])
C1706867 (UMLS CUI [2])
C0555954 (UMLS CUI [3])
therapy indication
Item
to have a need for therapy in the opinion of treating clinician
boolean
C0087111 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
measurable disease
Item
measurable disease
boolean
C1513041 (UMLS CUI [1])
life expectancy
Item
expected survival of 6 months or more
boolean
C0023671 (UMLS CUI [1])
age
Item
age 18 to 70 years
boolean
C0001779 (UMLS CUI [1])
chemotherapy
Item
to have undergone < 3 lines of chemotherapy
boolean
C0392920 (UMLS CUI [1])
performance status
Item
performance status of 0 to 2
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
hiv
Item
known hiv infections
boolean
C0019682 (UMLS CUI [1])
hepatitis b or c
Item
known hepatitis b or c
boolean
C0019163 (UMLS CUI [1])
C0019196 (UMLS CUI [2])
cns lymphoma
Item
cns lymphoma
boolean
C0280803 (UMLS CUI [1])
comorbidity
Item
previous malignancies, or cardiac, renal, hepatic, or respiratory failure
boolean
C0009488 (UMLS CUI [1])
pregnancy, lactation, contraception
Item
pregnant or lactating women and patients of child bearing potential unless using birth control measures
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [3])

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