Informações:
Falhas:
ID
13179
Descrição
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
Link
https://clinicaltrials.gov/show/NCT00004228
Palavras-chave
Versões (1)
- 21/01/2016 21/01/2016 -
Transferido a
21 de janeiro de 2016
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Lymphoma NCT00004228
Eligibility Lymphoma NCT00004228
- StudyEvent: Eligibility
Similar models
Eligibility Lymphoma NCT00004228
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
C0038833 (UMLS CUI [2])