Information:
Fel:
ID
39054
Beskrivning
Reduced Radiation in Patients With Diffuse Large B-cell Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT01186978
Länk
https://clinicaltrials.gov/show/NCT01186978
Nyckelord
Versioner (1)
- 2019-11-24 2019-11-24 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
24 november 2019
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Diffuse Large B-cell Lymphoma NCT01186978
Eligibility Diffuse Large B-cell Lymphoma NCT01186978
- StudyEvent: Eligibility
Similar models
Eligibility Diffuse Large B-cell Lymphoma NCT01186978
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
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])
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])
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])
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])
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])
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])
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])
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])
Medical contraindication Therapeutic radiology procedure
Item
any contraindications to irradiation
boolean
C1301624 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
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])
C0001175 (UMLS CUI [2])