ID

43825

Descripción

Prednisolone or Dexamethasone Combined With Chemotherapy in Treating Young Patients With Newly Diagnosed Lymphoblastic Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00275106

Link

https://clinicaltrials.gov/show/NCT00275106

Palabras clave

Versiones (3)
  1. 12/10/16 12/10/16 -
  2. 12/10/16 12/10/16 -
  3. 20/9/21 20/9/21 -
Subido en

20 de septiembre de 2021

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Lymphoma NCT00275106

Inglés

Eligibility Lymphoma NCT00275106

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00275106
Criteria
Descripción

Criteria

histologically or cytologically confirmed lymphoblastic lymphoma (lbl)
Descripción

adult lymphoblastic lymphoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0278721
stage i-iv disease
Descripción

TNM clinical staging

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3258246
t-cell lbl, precursor b-cell lbl, or lbl with an unknown immunophenotype
Descripción

Lymphoblastic T-cell lymphoma | Precursor B-cell lymphoblastic lymphoma | adult lymphoblastic lymphoma Immunophenotype Unknown

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2853920
UMLS CUI [2]
C0855146
UMLS CUI [3,1]
C0278721
UMLS CUI [3,2]
C0079611
UMLS CUI [3,3]
C0439673
patient characteristics:
Descripción

Client Characteristics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0815172
not pregnant or nursing
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
negative pregnancy test
Descripción

Pregnancy test negative

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0427780
fertile patients must use effective contraception during and for 3 months after completion of study treatment
Descripción

Fertility Contraceptive methods

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0015895
UMLS CUI [1,2]
C0700589
no known hiv or aids infection
Descripción

HIV Infection | Acquired Immunodeficiency Syndrome

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0001175
no severe immunodeficiency
Descripción

Immunologic Deficiency Syndrome Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021051
UMLS CUI [1,2]
C0205082
no other prior malignancy
Descripción

Malignant Neoplasms

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
no prior disease that would preclude treatment with chemotherapy
Descripción

Disease Excludes Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0392920
prior concurrent therapy:
Descripción

Prior Therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1514463
more than 2 months since prior systemic corticosteroids for a duration of > 8 days
Descripción

systemic steroids

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2825233
no prior chemotherapy
Descripción

Prior Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1514457
no prior radiotherapy
Descripción

prior radiation therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0279134
no prior organ transplant
Descripción

Organ Transplantation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0029216
no trimethoprim-sulfamethoxazole 6 days before or during methotrexate therapy
Descripción

Trimethoprim-Sulfamethoxazole Combination | Methotrexate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0041044
UMLS CUI [2]
C0025677
no concurrent participation in another clinical trial
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Lymphoma NCT00275106

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00275106
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
adult lymphoblastic lymphoma
Item
histologically or cytologically confirmed lymphoblastic lymphoma (lbl)
boolean
C0278721 (UMLS CUI [1])
TNM clinical staging
Item
stage i-iv disease
boolean
C3258246 (UMLS CUI [1])
Lymphoblastic T-cell lymphoma | Precursor B-cell lymphoblastic lymphoma | adult lymphoblastic lymphoma Immunophenotype Unknown
Item
t-cell lbl, precursor b-cell lbl, or lbl with an unknown immunophenotype
boolean
C2853920 (UMLS CUI [1])
C0855146 (UMLS CUI [2])
C0278721 (UMLS CUI [3,1])
C0079611 (UMLS CUI [3,2])
C0439673 (UMLS CUI [3,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Pregnancy test negative
Item
negative pregnancy test
boolean
C0427780 (UMLS CUI [1])
Fertility Contraceptive methods
Item
fertile patients must use effective contraception during and for 3 months after completion of study treatment
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
HIV Infection | Acquired Immunodeficiency Syndrome
Item
no known hiv or aids infection
boolean
C0019693 (UMLS CUI [1])
C0001175 (UMLS CUI [2])
Immunologic Deficiency Syndrome Severe
Item
no severe immunodeficiency
boolean
C0021051 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Malignant Neoplasms
Item
no other prior malignancy
boolean
C0006826 (UMLS CUI [1])
Disease Excludes Chemotherapy
Item
no prior disease that would preclude treatment with chemotherapy
boolean
C0012634 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
Prior Therapy
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1])
systemic steroids
Item
more than 2 months since prior systemic corticosteroids for a duration of > 8 days
boolean
C2825233 (UMLS CUI [1])
Prior Chemotherapy
Item
no prior chemotherapy
boolean
C1514457 (UMLS CUI [1])
prior radiation therapy
Item
no prior radiotherapy
boolean
C0279134 (UMLS CUI [1])
Organ Transplantation
Item
no prior organ transplant
boolean
C0029216 (UMLS CUI [1])
Trimethoprim-Sulfamethoxazole Combination | Methotrexate
Item
no trimethoprim-sulfamethoxazole 6 days before or during methotrexate therapy
boolean
C0041044 (UMLS CUI [1])
C0025677 (UMLS CUI [2])
Study Subject Participation Status
Item
no concurrent participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])
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