ID

13682

Description

Lenalidomide Plus Bendamustine and Rituximab for Untreated CLL/SLL; ODM derived from: https://clinicaltrials.gov/show/NCT01400685

Lien

https://clinicaltrials.gov/show/NCT01400685

Mots-clés

  1. 28/02/2016 28/02/2016 -
Téléchargé le

28 février 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Chronic Lymphocytic Leukemia NCT01400685

Eligibility Chronic Lymphocytic Leukemia NCT01400685

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosed with b-cell cll or sll (chronic lymphocytic leukemia or small lymphocytic leukemia)
Description

Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Type de données

boolean

Alias
UMLS CUI [1]
C1302547
life expectancy > 3 months
Description

life expectancy

Type de données

boolean

Alias
UMLS CUI [1]
C0023671
organ and marrow function with protocol parameters
Description

organ function bone marrow

Type de données

boolean

Alias
UMLS CUI [1,1]
C0678852
UMLS CUI [1,2]
C0005953
able to take aspirin daily
Description

aspirin

Type de données

boolean

Alias
UMLS CUI [1]
C0004057
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
age >80 years
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
prior systemic therapy for cll/sll including chemotherapy or antibody therapy
Description

systemic therapy Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphom; antibody therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C1515119
UMLS CUI [1,2]
C1302547
UMLS CUI [2]
C0281176
pregnant or breast-feeding
Description

pregnant; lactating

Type de données

boolean

Alias
UMLS CUI [1]
C0549206
UMLS CUI [2]
C2828358
serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing informed consent
Description

Informed Consent Limited Comorbidity

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
known hypersensitivity to thalidomide or lenalidomide
Description

hypersensitivity thalidomide

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0039736
prior use of lenalidomide
Description

lenalidomide

Type de données

boolean

Alias
UMLS CUI [1]
C1144149
concurrent use of other anti-cancer agents or treatments
Description

concurrent therapy Antineoplastic Agents

Type de données

boolean

Alias
UMLS CUI [1,1]
C0009429
UMLS CUI [1,2]
C0003392
hiv positive
Description

hiv positive

Type de données

boolean

Alias
UMLS CUI [1]
C0019699
prior history of another malignancy unless disease free for at least 2 years
Description

medical history Malignant Neoplasms

Type de données

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0006826
uncontrolled intercurrent illness
Description

intercurrent illness

Type de données

boolean

Alias
UMLS CUI [1]
C3640977

Similar models

Eligibility Chronic Lymphocytic Leukemia NCT01400685

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Item
diagnosed with b-cell cll or sll (chronic lymphocytic leukemia or small lymphocytic leukemia)
boolean
C1302547 (UMLS CUI [1])
life expectancy
Item
life expectancy > 3 months
boolean
C0023671 (UMLS CUI [1])
organ function bone marrow
Item
organ and marrow function with protocol parameters
boolean
C0678852 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
aspirin
Item
able to take aspirin daily
boolean
C0004057 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
age
Item
age >80 years
boolean
C0001779 (UMLS CUI [1])
systemic therapy Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphom; antibody therapy
Item
prior systemic therapy for cll/sll including chemotherapy or antibody therapy
boolean
C1515119 (UMLS CUI [1,1])
C1302547 (UMLS CUI [1,2])
C0281176 (UMLS CUI [2])
pregnant; lactating
Item
pregnant or breast-feeding
boolean
C0549206 (UMLS CUI [1])
C2828358 (UMLS CUI [2])
Informed Consent Limited Comorbidity
Item
serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
hypersensitivity thalidomide
Item
known hypersensitivity to thalidomide or lenalidomide
boolean
C0020517 (UMLS CUI [1,1])
C0039736 (UMLS CUI [1,2])
lenalidomide
Item
prior use of lenalidomide
boolean
C1144149 (UMLS CUI [1])
concurrent therapy Antineoplastic Agents
Item
concurrent use of other anti-cancer agents or treatments
boolean
C0009429 (UMLS CUI [1,1])
C0003392 (UMLS CUI [1,2])
hiv positive
Item
hiv positive
boolean
C0019699 (UMLS CUI [1])
medical history Malignant Neoplasms
Item
prior history of another malignancy unless disease free for at least 2 years
boolean
C0262926 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
intercurrent illness
Item
uncontrolled intercurrent illness
boolean
C3640977 (UMLS CUI [1])

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