ID

12991

Description

Treatment of Mature B-cell Lymphoma/Leukaemia; ODM derived from: https://clinicaltrials.gov/show/NCT00162656

Lien

https://clinicaltrials.gov/show/NCT00162656

Mots-clés

  1. 10/01/2016 10/01/2016 -
Téléchargé le

10 janvier 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility B-Cell Lymphoma NCT00162656

Eligibility B-Cell Lymphoma NCT00162656

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
newly diagnosed b lineage non-hodgkin's lymphoma with revised european american lymphoma (real) ii 9 (diffuse large cell lymphoma), 10 (burkitt's lymphoma), or 11 (high grade b cell lymphoma, burkitt's like) or bone marrow > 5% l3 blasts.
Description

B-NHL, Diffuse large cell, Burkitt, High grade, burkitt-like lymphoma, bone marrow blasts

Type de données

boolean

Alias
UMLS CUI [1]
C0079731
UMLS CUI [2]
C0024305
UMLS CUI [3]
C0079744
UMLS CUI [4]
C0456863
UMLS CUI [5]
C0006413
UMLS CUI [6]
C1368771
UMLS CUI [7]
C1982687
pre treatment imaging studies adequate to document murphy disease stage
Description

murphy disease stage

Type de données

boolean

Alias
UMLS CUI [1]
C0699749
group b and c patients are eligible for randomization (therapy stratification by group : group a=completely resected stage i or completely resected abdominal stage ii lesions, group b= all cases not eligible for group a or group c, group c= any cns involvement and/or bone marrow involvement ³ 25% blasts)
Description

randomization

Type de données

boolean

Alias
UMLS CUI [1]
C0034656
patients should be available for a minimum follow up of 36 months
Description

Follow up

Type de données

boolean

Alias
UMLS CUI [1]
C1522577
informed consent prior to study entry
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
anaplastic large cell ki 1 positive lymphomas
Description

anaplastic large cell ki 1 positive lymphomas

Type de données

boolean

Alias
UMLS CUI [1]
C0206180
previous chemotherapy.
Description

chemotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C0392920
congenital immunodeficiency
Description

congenital immunodeficiency

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021051
UMLS CUI [1,2]
C0853602
prior organ transplantation
Description

organ transplantation

Type de données

boolean

Alias
UMLS CUI [1]
C0029216
previous malignancy of any type
Description

malignancy

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
known hiv positivity
Description

hiv positivity

Type de données

boolean

Alias
UMLS CUI [1]
C0019699

Similar models

Eligibility B-Cell Lymphoma NCT00162656

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
B-NHL, Diffuse large cell, Burkitt, High grade, burkitt-like lymphoma, bone marrow blasts
Item
newly diagnosed b lineage non-hodgkin's lymphoma with revised european american lymphoma (real) ii 9 (diffuse large cell lymphoma), 10 (burkitt's lymphoma), or 11 (high grade b cell lymphoma, burkitt's like) or bone marrow > 5% l3 blasts.
boolean
C0079731 (UMLS CUI [1])
C0024305 (UMLS CUI [2])
C0079744 (UMLS CUI [3])
C0456863 (UMLS CUI [4])
C0006413 (UMLS CUI [5])
C1368771 (UMLS CUI [6])
C1982687 (UMLS CUI [7])
murphy disease stage
Item
pre treatment imaging studies adequate to document murphy disease stage
boolean
C0699749 (UMLS CUI [1])
randomization
Item
group b and c patients are eligible for randomization (therapy stratification by group : group a=completely resected stage i or completely resected abdominal stage ii lesions, group b= all cases not eligible for group a or group c, group c= any cns involvement and/or bone marrow involvement ³ 25% blasts)
boolean
C0034656 (UMLS CUI [1])
Follow up
Item
patients should be available for a minimum follow up of 36 months
boolean
C1522577 (UMLS CUI [1])
informed consent
Item
informed consent prior to study entry
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
anaplastic large cell ki 1 positive lymphomas
Item
anaplastic large cell ki 1 positive lymphomas
boolean
C0206180 (UMLS CUI [1])
chemotherapy
Item
previous chemotherapy.
boolean
C0392920 (UMLS CUI [1])
congenital immunodeficiency
Item
congenital immunodeficiency
boolean
C0021051 (UMLS CUI [1,1])
C0853602 (UMLS CUI [1,2])
organ transplantation
Item
prior organ transplantation
boolean
C0029216 (UMLS CUI [1])
malignancy
Item
previous malignancy of any type
boolean
C0006826 (UMLS CUI [1])
hiv positivity
Item
known hiv positivity
boolean
C0019699 (UMLS CUI [1])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial