ID

12617

Description

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

Keywords

Versions (1)
  1. 12/6/15 12/6/15 -
Uploaded on

December 6, 2015

DOI

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License

Creative Commons BY 4.0
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Eligibility AIDS Related Lymphoma NCT00001563

English

Eligibility AIDS Related Lymphoma NCT00001563

1 forms  
Criteria
Description

Criteria

aggressive cd20 + nhl confirmed by pathology, dcs.
Description

aggressive cd20 + nhl confirmed by pathology, dcs.

Data type

text

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

HIV

Data type

boolean

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

all stages (i-iv) of disease.

Data type

boolean

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

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

Data type

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.
Description

Age

Data type

boolean

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

ID.6

Data type

boolean

creatinine less than or equal to 1.7.
Description

creatinine levels

Data type

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.
Description

Bilirubin levels

Data type

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).
Description

AST and ALT levels

Data type

boolean

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

Absolute neutrophil count

Data type

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).
Description

Platelet count

Data type

boolean

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

signed informed consent and durable power of attorney.

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
Pregnancy or nursing
Description

Pregnancy or nursing.

Data type

boolean

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

history of clinical heart failure or symptomatic ischemic heart disease.

Data type

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.
Description

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

Data type

boolean

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

concurrent anti-retroviral therapy during epoch therapy.

Data type

boolean

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

primary cns lymphoma.

Data type

boolean

Alias
UMLS CUI [1]
C0280803
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Similar models

Eligibility AIDS Related Lymphoma NCT00001563

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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