ID

14460

Description

Treatment of Acute Lymphoblastic Leukemia or Aggressive Lymphoma With Relapse in Central Nervous System With Depocyt; ODM derived from: https://clinicaltrials.gov/show/NCT00199108

Link

https://clinicaltrials.gov/show/NCT00199108

Keywords

  1. 4/16/16 4/16/16 -
Uploaded on

April 16, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Adult Acute Lymphocytic Leukemia NCT00199108

Eligibility Adult Acute Lymphocytic Leukemia NCT00199108

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
proven diagnosis of all or very aggressive non-hodgkin-lymphoma (burkitt/burkitt-like) and cns relapse
Description

all or non-hodgkin-lymphoma

Data type

boolean

Alias
UMLS CUI [1]
C0023449
UMLS CUI [2]
C0006413
cns involvement demonstrated by a positive ventricular or lumbar csf cytology or characteristic signs and symptoms of neoplastic meningitis plus an mri or ct scan indicating the presence of meningeal involvement
Description

cns involvement

Data type

boolean

Alias
UMLS CUI [1]
C0449389
in combined relapse in cns and other locations: systemic therapy with cns active drugs can be postponed for at least 2 weeks
Description

systemic therapy

Data type

boolean

Alias
UMLS CUI [1]
C1515119
karnofsky performance score is > or = 60%
Description

karnofsky performance score

Data type

boolean

Alias
UMLS CUI [1]
C0206065
18 years of age or older
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
free of uncontrolled infection
Description

Communicable Diseases

Data type

boolean

Alias
UMLS CUI [1]
C0009450
recovered from any grade iii / iv toxicities attributable to prior treatment with the exception of hematotoxicity
Description

Drug toxicity

Data type

boolean

Alias
UMLS CUI [1]
C0013221
patient not pregnant or breast feeding and effective methods to prevent pregnancy
Description

Not pregnant or breast feeding

Data type

boolean

Alias
UMLS CUI [1]
C3242212
UMLS CUI [2]
C0700589
free from severe heart, lung, liver or kidney dysfunction
Description

Multiple Organ Failure

Data type

boolean

Alias
UMLS CUI [1]
C0026766
written informed consent
Description

written informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
failed to respond (as defined by no clearance of the csf) to > 1 dose of prior i.th. mtx or arac or triple therapy
Description

Methotrexate

Data type

boolean

Alias
UMLS CUI [1]
C0025677
history of neurotoxicity (grade iii - iv) attributed to i.th. or systemic hd therapy with mtx or arac
Description

Neurotoxicity Syndromes

Data type

boolean

Alias
UMLS CUI [1]
C0235032
prior cns relapse < 1 month before
Description

cns relapse

Data type

boolean

Alias
UMLS CUI [1,1]
C3714787
UMLS CUI [1,2]
C0035020

Similar models

Eligibility Adult Acute Lymphocytic Leukemia NCT00199108

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
all or non-hodgkin-lymphoma
Item
proven diagnosis of all or very aggressive non-hodgkin-lymphoma (burkitt/burkitt-like) and cns relapse
boolean
C0023449 (UMLS CUI [1])
C0006413 (UMLS CUI [2])
cns involvement
Item
cns involvement demonstrated by a positive ventricular or lumbar csf cytology or characteristic signs and symptoms of neoplastic meningitis plus an mri or ct scan indicating the presence of meningeal involvement
boolean
C0449389 (UMLS CUI [1])
systemic therapy
Item
in combined relapse in cns and other locations: systemic therapy with cns active drugs can be postponed for at least 2 weeks
boolean
C1515119 (UMLS CUI [1])
karnofsky performance score
Item
karnofsky performance score is > or = 60%
boolean
C0206065 (UMLS CUI [1])
Age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Communicable Diseases
Item
free of uncontrolled infection
boolean
C0009450 (UMLS CUI [1])
Drug toxicity
Item
recovered from any grade iii / iv toxicities attributable to prior treatment with the exception of hematotoxicity
boolean
C0013221 (UMLS CUI [1])
Not pregnant or breast feeding
Item
patient not pregnant or breast feeding and effective methods to prevent pregnancy
boolean
C3242212 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
Multiple Organ Failure
Item
free from severe heart, lung, liver or kidney dysfunction
boolean
C0026766 (UMLS CUI [1])
written informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Methotrexate
Item
failed to respond (as defined by no clearance of the csf) to > 1 dose of prior i.th. mtx or arac or triple therapy
boolean
C0025677 (UMLS CUI [1])
Neurotoxicity Syndromes
Item
history of neurotoxicity (grade iii - iv) attributed to i.th. or systemic hd therapy with mtx or arac
boolean
C0235032 (UMLS CUI [1])
cns relapse
Item
prior cns relapse < 1 month before
boolean
C3714787 (UMLS CUI [1,1])
C0035020 (UMLS CUI [1,2])

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