ID

13179

Descrizione

Combination Chemotx in Treating Children or Adolescents With Newly Diagnosed Stg III or Stg IV Lymphoblastic Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00004228

collegamento

https://clinicaltrials.gov/show/NCT00004228

Keywords

  1. 21/01/16 21/01/16 -
Caricato su

21 gennaio 2016

DOI

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Licenza

Creative Commons BY 4.0

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Eligibility Lymphoma NCT00004228

Eligibility Lymphoma NCT00004228

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00004228
Criteria
Descrizione

Criteria

newly diagnosed disseminated lymphoblastic lymphoma or localized lymphoblastic lymphoma* note: *localized lymphoblastic lymphoma is closed to accrual as of 10/2005
Descrizione

lymphoblastic lymphoma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0024299
less than 25% tumor cells in the bone marrow
Descrizione

bone marrow

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0005953
previously untreated (prior intrathecal cytarabine allowed if protocol therapy begins within 72 hours)
Descrizione

therapy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0087111
stage iii or iv disease
Descrizione

disease stage

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0699749
age: 1 to 30
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
cardiovascular: adequate cardiac function
Descrizione

cardiac function

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0232164
prior concurrent therapy: endocrine therapy: emergency steroid therapy (if required) must be started within 72 hours prior to protocol therapy
Descrizione

steroid therapy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0149783
prior concurrent therapy: radiotherapy: emergency radiotherapy (if required) must be started within 72 hours prior to protocol therapy
Descrizione

radiotherapy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1522449
other: no other prior therapy except for emergency treatment of airway obstruction and/or superior vena cava syndrome
Descrizione

airway obstruction, superior vena cava syndrome

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001883
UMLS CUI [2]
C0038833

Similar models

Eligibility Lymphoma NCT00004228

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00004228
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
lymphoblastic lymphoma
Item
newly diagnosed disseminated lymphoblastic lymphoma or localized lymphoblastic lymphoma* note: *localized lymphoblastic lymphoma is closed to accrual as of 10/2005
boolean
C0024299 (UMLS CUI [1])
bone marrow
Item
less than 25% tumor cells in the bone marrow
boolean
C0005953 (UMLS CUI [1])
therapy
Item
previously untreated (prior intrathecal cytarabine allowed if protocol therapy begins within 72 hours)
boolean
C0087111 (UMLS CUI [1])
disease stage
Item
stage iii or iv disease
boolean
C0699749 (UMLS CUI [1])
age
Item
age: 1 to 30
boolean
C0001779 (UMLS CUI [1])
cardiac function
Item
cardiovascular: adequate cardiac function
boolean
C0232164 (UMLS CUI [1])
steroid therapy
Item
prior concurrent therapy: endocrine therapy: emergency steroid therapy (if required) must be started within 72 hours prior to protocol therapy
boolean
C0149783 (UMLS CUI [1])
radiotherapy
Item
prior concurrent therapy: radiotherapy: emergency radiotherapy (if required) must be started within 72 hours prior to protocol therapy
boolean
C1522449 (UMLS CUI [1])
airway obstruction, superior vena cava syndrome
Item
other: no other prior therapy except for emergency treatment of airway obstruction and/or superior vena cava syndrome
boolean
C0001883 (UMLS CUI [1])
C0038833 (UMLS CUI [2])

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