ID

39054

Descripción

Reduced Radiation in Patients With Diffuse Large B-cell Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT01186978

Link

https://clinicaltrials.gov/show/NCT01186978

Palabras clave

Versiones (1)
  1. 24/11/19 24/11/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

24 de noviembre de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Diffuse Large B-cell Lymphoma NCT01186978

Inglés

Eligibility Diffuse Large B-cell Lymphoma NCT01186978

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologic documentation of diffuse large b-cell lymphoma, or any of its variants as defined in the who classification
Descripción

Diffuse Large B-Cell Lymphoma WHO tumor classification | Diffuse Large B-Cell Lymphoma Variant WHO tumor classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0079744
UMLS CUI [1,2]
C1301142
UMLS CUI [2,1]
C0079744
UMLS CUI [2,2]
C0205419
UMLS CUI [2,3]
C1301142
completion of at least 4 cycles of a rituximab-containing, anthracycline-based combination chemotherapy
Descripción

Chemotherapy cycle Quantity Completion | Chemotherapy Containing Rituximab | Combination Chemotherapy Anthracycline Based

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0205197
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0332256
UMLS CUI [2,3]
C0393022
UMLS CUI [3,1]
C1521750
UMLS CUI [3,2]
C0282564
UMLS CUI [3,3]
C1705938
negative post-chemotherapy (or interim) pet scan
Descripción

PET scan Negative | Status post Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032743
UMLS CUI [1,2]
C1513916
UMLS CUI [2,1]
C0231290
UMLS CUI [2,2]
C0392920
absolute neutrophil count greater than 1500 and platelet count greater than 40,000
Descripción

Absolute neutrophil count | Platelet Count measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0948762
UMLS CUI [2]
C0032181
negative pregnancy test in women of child-bearing potential
Descripción

Childbearing Potential Pregnancy test negative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0427780
for patients with hiv/aids, the following must be true:
Descripción

Patients HIV Infection | Patients AIDS

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0019693
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C0001175
the patient is compliant on combination anti-retroviral therapy (cart)
Descripción

Compliance behavior Combination Antiretroviral therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0205195
UMLS CUI [1,3]
C1963724
the patient has cd4 count ≥ 200 at time of diagnosis
Descripción

CD4 Count determination

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0243009
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
any contraindications to irradiation
Descripción

Medical contraindication Therapeutic radiology procedure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1522449
primary cns lymphoma
Descripción

Primary central nervous system lymphoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0280803
hiv/aids
Descripción

HIV Infection | AIDS

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0001175
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Similar models

Eligibility Diffuse Large B-cell Lymphoma NCT01186978

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Diffuse Large B-Cell Lymphoma WHO tumor classification | Diffuse Large B-Cell Lymphoma Variant WHO tumor classification
Item
histologic documentation of diffuse large b-cell lymphoma, or any of its variants as defined in the who classification
boolean
C0079744 (UMLS CUI [1,1])
C1301142 (UMLS CUI [1,2])
C0079744 (UMLS CUI [2,1])
C0205419 (UMLS CUI [2,2])
C1301142 (UMLS CUI [2,3])
Chemotherapy cycle Quantity Completion | Chemotherapy Containing Rituximab | Combination Chemotherapy Anthracycline Based
Item
completion of at least 4 cycles of a rituximab-containing, anthracycline-based combination chemotherapy
boolean
C1302181 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
C0392920 (UMLS CUI [2,1])
C0332256 (UMLS CUI [2,2])
C0393022 (UMLS CUI [2,3])
C1521750 (UMLS CUI [3,1])
C0282564 (UMLS CUI [3,2])
C1705938 (UMLS CUI [3,3])
PET scan Negative | Status post Chemotherapy
Item
negative post-chemotherapy (or interim) pet scan
boolean
C0032743 (UMLS CUI [1,1])
C1513916 (UMLS CUI [1,2])
C0231290 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
Absolute neutrophil count | Platelet Count measurement
Item
absolute neutrophil count greater than 1500 and platelet count greater than 40,000
boolean
C0948762 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
Childbearing Potential Pregnancy test negative
Item
negative pregnancy test in women of child-bearing potential
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
Patients HIV Infection | Patients AIDS
Item
for patients with hiv/aids, the following must be true:
boolean
C0030705 (UMLS CUI [1,1])
C0019693 (UMLS CUI [1,2])
C0030705 (UMLS CUI [2,1])
C0001175 (UMLS CUI [2,2])
Compliance behavior Combination Antiretroviral therapy
Item
the patient is compliant on combination anti-retroviral therapy (cart)
boolean
C1321605 (UMLS CUI [1,1])
C0205195 (UMLS CUI [1,2])
C1963724 (UMLS CUI [1,3])
CD4 Count determination
Item
the patient has cd4 count ≥ 200 at time of diagnosis
boolean
C0243009 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Therapeutic radiology procedure
Item
any contraindications to irradiation
boolean
C1301624 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
Primary central nervous system lymphoma
Item
primary cns lymphoma
boolean
C0280803 (UMLS CUI [1])
HIV Infection | AIDS
Item
hiv/aids
boolean
C0019693 (UMLS CUI [1])
C0001175 (UMLS CUI [2])
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