Eligibility Non-Hodgkin's Lymphoma NCT00576758

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, >=18 years of age
Descrição

Adult | Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C0001779
relapsed cd20+ indolent b-cell non-hodgkin's lymphoma
Descrição

B-cell lymphoma recurrent CD20 positive indolent

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0855089
UMLS CUI [1,2]
C3888518
UMLS CUI [1,3]
C0234227
documented history of response of >/= 6 months duration from last rituximab-containing regimen
Descrição

Disease Response Due to Rituximab therapy

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1704632
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C4047978
clinical indication for treatment as determined by the investigator
Descrição

Indication Therapeutic procedure

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0087111
eastern cooperative oncology group (ecog) performance status 0-2
Descrição

ECOG performance status

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior use of any investigational monoclonal antibody within 6 months of study start
Descrição

Monoclonal Antibodies Investigational

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0003250
UMLS CUI [1,2]
C1517586
prior use of any anti-cancer vaccine
Descrição

Cancer Vaccines

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0376659
prior use of rituximab within 8 weeks of study entry
Descrição

Rituximab Use of Previous

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0393022
UMLS CUI [1,2]
C1524063
UMLS CUI [1,3]
C0205156
radioimmunotherapy within 3 months prior to study entry
Descrição

Radioimmunotherapy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0085101
central nervous system (cns) lymphoma or evidence of transformation to high-grade or diffuse large b-cell lymphoma
Descrição

Central nervous system lymphoma | Transformation High grade B-cell lymphoma | Transformation Diffuse Large B-Cell Lymphoma

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0742472
UMLS CUI [2,1]
C0040682
UMLS CUI [2,2]
C0456863
UMLS CUI [3,1]
C0040682
UMLS CUI [3,2]
C0079744

Similar models

Eligibility Non-Hodgkin's Lymphoma NCT00576758

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Age
Item
adult patients, >=18 years of age
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
B-cell lymphoma recurrent CD20 positive indolent
Item
relapsed cd20+ indolent b-cell non-hodgkin's lymphoma
boolean
C0855089 (UMLS CUI [1,1])
C3888518 (UMLS CUI [1,2])
C0234227 (UMLS CUI [1,3])
Disease Response Due to Rituximab therapy
Item
documented history of response of >/= 6 months duration from last rituximab-containing regimen
boolean
C1704632 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C4047978 (UMLS CUI [1,3])
Indication Therapeutic procedure
Item
clinical indication for treatment as determined by the investigator
boolean
C3146298 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
ECOG performance status
Item
eastern cooperative oncology group (ecog) performance status 0-2
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Monoclonal Antibodies Investigational
Item
prior use of any investigational monoclonal antibody within 6 months of study start
boolean
C0003250 (UMLS CUI [1,1])
C1517586 (UMLS CUI [1,2])
Cancer Vaccines
Item
prior use of any anti-cancer vaccine
boolean
C0376659 (UMLS CUI [1])
Rituximab Use of Previous
Item
prior use of rituximab within 8 weeks of study entry
boolean
C0393022 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
Radioimmunotherapy
Item
radioimmunotherapy within 3 months prior to study entry
boolean
C0085101 (UMLS CUI [1])
Central nervous system lymphoma | Transformation High grade B-cell lymphoma | Transformation Diffuse Large B-Cell Lymphoma
Item
central nervous system (cns) lymphoma or evidence of transformation to high-grade or diffuse large b-cell lymphoma
boolean
C0742472 (UMLS CUI [1])
C0040682 (UMLS CUI [2,1])
C0456863 (UMLS CUI [2,2])
C0040682 (UMLS CUI [3,1])
C0079744 (UMLS CUI [3,2])