ID

12617

Beschrijving

EPOCH Chemotherapy +/- IL-12 for Previously Untreated and EPOCH Plus Rituximab for Previously Treated Patients With AIDS-Associated Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00001563

Link

https://clinicaltrials.gov/show/NCT00001563

Trefwoorden

Versies (1)
  1. 06-12-15 06-12-15 -
Geüploaded op

6 december 2015

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility AIDS Related Lymphoma NCT00001563

Engels

Eligibility AIDS Related Lymphoma NCT00001563

1 Formulieren  
Criteria
Beschrijving

Criteria

aggressive cd20 + nhl confirmed by pathology, dcs.
Beschrijving

aggressive cd20 + nhl confirmed by pathology, dcs.

Datatype

text

Alias
UMLS CUI [1,1]
C0852469
UMLS CUI [1,2]
C0882818
UMLS CUI [1,3]
C0679557
hiv + serology.
Beschrijving

HIV

Datatype

boolean

Alias
UMLS CUI [1]
C0019699
all stages (i-iv) of disease.
Beschrijving

all stages (i-iv) of disease.

Datatype

boolean

Alias
UMLS CUI [1]
C0019699
nhl previously treated with up to two chemotherapy regimens and evaluable disease.
Beschrijving

nhl previously treated with up to two chemotherapy regimens and evaluable disease.

Datatype

boolean

Alias
UMLS CUI [1,1]
C0852469
UMLS CUI [1,2]
C1514457
UMLS CUI [1,3]
C1516986
age greater than or equal to 18 years.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
laboratory test: (abnormalities are allowed if due to organ involvement by lymphoma).
Beschrijving

ID.6

Datatype

boolean

creatinine less than or equal to 1.7.
Beschrijving

creatinine levels

Datatype

boolean

Alias
UMLS CUI [1]
C1561535
bilirubin must be less than 2.0 mg/dl, or total bilirubin less than or equal to 3.7 mg/dl with direct fraction less than or equal to 0.2 mg/dl and indirect fraction of less than or equal 3.5 mg/dl in patients for whom these abnormalities are felt to be due to protease inhibitor therapy.
Beschrijving

Bilirubin levels

Datatype

boolean

Alias
UMLS CUI [1]
C1557209
ast and alt less than or equal to 3 times uln (ast and alt less than or equal to 6 times uln for patients on hyperalimentation for whom these abnormalities are felt to be due to the hyperalimentation).
Beschrijving

AST and ALT levels

Datatype

boolean

Alias
UMLS CUI [1]
C0201836
UMLS CUI [2]
C0201899
anc greater than or equal 1000/mm(3).
Beschrijving

Absolute neutrophil count

Datatype

boolean

Alias
UMLS CUI [1]
C0948762
platelets must be greater than or equal to 75,000/mm(3) (patients with itp platelets greater than or equal to 30,000/mm(3).
Beschrijving

Platelet count

Datatype

boolean

Alias
UMLS CUI [1]
C0005821
signed informed consent and durable power of attorney.
Beschrijving

signed informed consent and durable power of attorney.

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
Pregnancy or nursing
Beschrijving

Pregnancy or nursing.

Datatype

boolean

Alias
UMLS CUI [1,1]
C0549206
UMLS CUI [1,2]
C0006147
history of clinical heart failure or symptomatic ischemic heart disease.
Beschrijving

history of clinical heart failure or symptomatic ischemic heart disease.

Datatype

boolean

Alias
UMLS CUI [1,1]
C2004062
UMLS CUI [1,2]
C0018801
UMLS CUI [1,3]
C0151744
serious underlying medical condition or infection other than hiv that would contraindicate epoch.
Beschrijving

serious underlying medical condition or infection other than hiv that would contraindicate epoch.

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C1301624
UMLS CUI [1,3]
C2946699
concurrent anti-retroviral therapy during epoch therapy.
Beschrijving

concurrent anti-retroviral therapy during epoch therapy.

Datatype

boolean

Alias
UMLS CUI [1,1]
C0205420
UMLS CUI [1,2]
C1963724
primary cns lymphoma.
Beschrijving

primary cns lymphoma.

Datatype

boolean

Alias
UMLS CUI [1]
C0280803
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Similar models

Eligibility AIDS Related Lymphoma NCT00001563

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
aggressive cd20 + nhl confirmed by pathology, dcs.
Item
aggressive cd20 + nhl confirmed by pathology, dcs.
text
C0852469 (UMLS CUI [1,1])
C0882818 (UMLS CUI [1,2])
C0679557 (UMLS CUI [1,3])
HIV
Item
hiv + serology.
boolean
C0019699 (UMLS CUI [1])
all stages (i-iv) of disease.
Item
all stages (i-iv) of disease.
boolean
C0019699 (UMLS CUI [1])
nhl previously treated with up to two chemotherapy regimens and evaluable disease.
Item
nhl previously treated with up to two chemotherapy regimens and evaluable disease.
boolean
C0852469 (UMLS CUI [1,1])
C1514457 (UMLS CUI [1,2])
C1516986 (UMLS CUI [1,3])
Age
Item
age greater than or equal to 18 years.
boolean
C0001779 (UMLS CUI [1])
ID.6
Item
laboratory test: (abnormalities are allowed if due to organ involvement by lymphoma).
boolean
creatinine levels
Item
creatinine less than or equal to 1.7.
boolean
C1561535 (UMLS CUI [1])
Bilirubin levels
Item
bilirubin must be less than 2.0 mg/dl, or total bilirubin less than or equal to 3.7 mg/dl with direct fraction less than or equal to 0.2 mg/dl and indirect fraction of less than or equal 3.5 mg/dl in patients for whom these abnormalities are felt to be due to protease inhibitor therapy.
boolean
C1557209 (UMLS CUI [1])
AST and ALT levels
Item
ast and alt less than or equal to 3 times uln (ast and alt less than or equal to 6 times uln for patients on hyperalimentation for whom these abnormalities are felt to be due to the hyperalimentation).
boolean
C0201836 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
Absolute neutrophil count
Item
anc greater than or equal 1000/mm(3).
boolean
C0948762 (UMLS CUI [1])
Platelet count
Item
platelets must be greater than or equal to 75,000/mm(3) (patients with itp platelets greater than or equal to 30,000/mm(3).
boolean
C0005821 (UMLS CUI [1])
signed informed consent and durable power of attorney.
Item
signed informed consent and durable power of attorney.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pregnancy or nursing.
Item
Pregnancy or nursing
boolean
C0549206 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
history of clinical heart failure or symptomatic ischemic heart disease.
Item
history of clinical heart failure or symptomatic ischemic heart disease.
boolean
C2004062 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C0151744 (UMLS CUI [1,3])
serious underlying medical condition or infection other than hiv that would contraindicate epoch.
Item
serious underlying medical condition or infection other than hiv that would contraindicate epoch.
boolean
C0009488 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C2946699 (UMLS CUI [1,3])
concurrent anti-retroviral therapy during epoch therapy.
Item
concurrent anti-retroviral therapy during epoch therapy.
boolean
C0205420 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
primary cns lymphoma.
Item
primary cns lymphoma.
boolean
C0280803 (UMLS CUI [1])
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