ID

30310

Beschrijving

Observational Controlled Clinical Trials, on Adult Patients With T-lymphoblastic Lymphoma Treated With Intensive Chemo/Radiotherapy or Intensive Chemotherapy Followed by Transplant. Evaluation of Clinical, Anatomy -Pathological Parameters; ODM derived from: https://clinicaltrials.gov/show/NCT00882011

Link

https://clinicaltrials.gov/show/NCT00882011

Trefwoorden

Versies (2)
  1. 28-05-18 28-05-18 -
  2. 28-05-18 28-05-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

28 mei 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Lymphoblastic Lymphoma NCT00882011

Engels

Eligibility Lymphoblastic Lymphoma NCT00882011

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
no previous therapy, except for treatments to face up to clinical presentation of emergency;
Beschrijving

Prior Therapy Absent | Exception Emergency treatment

Datatype

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0013969
medical history initially characterized by nodal mass/masses;
Beschrijving

Medical History Nodal mass

Datatype

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0746921
histological and immunophenotypic diagnosis that documents the diagnosis of t-lbl; in cases of bone marrow involvement and difficulties in obtaining nodal material, diagnosis could be based on bone marrow;
Beschrijving

T-cell lymphoblastic lymphoma Immunophenotyping | Bone Marrow Involvement Bone Marrow Examination

Datatype

boolean

Alias
UMLS CUI [1,1]
C1292758
UMLS CUI [1,2]
C0079611
UMLS CUI [2,1]
C1517677
UMLS CUI [2,2]
C0005957
availability of biological material for the study of tcr and gene-profile;
Beschrijving

Biospecimen Study T-Cell Receptor | Biospecimen Study Gene Expression Profile

Datatype

boolean

Alias
UMLS CUI [1,1]
C2347026
UMLS CUI [1,2]
C2603343
UMLS CUI [1,3]
C0034790
UMLS CUI [2,1]
C2347026
UMLS CUI [2,2]
C2603343
UMLS CUI [2,3]
C1956267
age ≥ 15 years;
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
all stages;
Beschrijving

Stages All

Datatype

boolean

Alias
UMLS CUI [1,1]
C1300072
UMLS CUI [1,2]
C0444868
infiltrated bone marrow <25%;
Beschrijving

Bone marrow infiltration Percent

Datatype

boolean

Alias
UMLS CUI [1,1]
C3854434
UMLS CUI [1,2]
C0439165
normal liver, renal and cardiac functions, except for alterations directly related to lymphoma;
Beschrijving

Liver function | Renal function | Cardiac function | Exception Alteration Relationship Lymphoma

Datatype

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0232804
UMLS CUI [3]
C0232164
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C1515926
UMLS CUI [4,3]
C0439849
UMLS CUI [4,4]
C0024299
estimates of treatment according to one of the last generation schedules;
Beschrijving

Treatment Schedule Generation Last

Datatype

boolean

Alias
UMLS CUI [1,1]
C0039798
UMLS CUI [1,2]
C0040808
UMLS CUI [1,3]
C0079411
UMLS CUI [1,4]
C1517741
written informed consent.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with previous hcv, hbsag+ or suffering from hiv;
Beschrijving

Hepatitis C | Hepatitis B surface antigen positive | HIV Infection

Datatype

boolean

Alias
UMLS CUI [1]
C0019196
UMLS CUI [2]
C0149709
UMLS CUI [3]
C0019693
patients with organic pathology not related to lymphoma.
Beschrijving

Organic disease Independent of Lymphoma

Datatype

boolean

Alias
UMLS CUI [1,1]
C0683324
UMLS CUI [1,2]
C0332291
UMLS CUI [1,3]
C0024299
Terug naar het begin van de pagina

Similar models

Eligibility Lymphoblastic Lymphoma NCT00882011

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Prior Therapy Absent | Exception Emergency treatment
Item
no previous therapy, except for treatments to face up to clinical presentation of emergency;
boolean
C1514463 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0013969 (UMLS CUI [2,2])
Medical History Nodal mass
Item
medical history initially characterized by nodal mass/masses;
boolean
C0262926 (UMLS CUI [1,1])
C0746921 (UMLS CUI [1,2])
T-cell lymphoblastic lymphoma Immunophenotyping | Bone Marrow Involvement Bone Marrow Examination
Item
histological and immunophenotypic diagnosis that documents the diagnosis of t-lbl; in cases of bone marrow involvement and difficulties in obtaining nodal material, diagnosis could be based on bone marrow;
boolean
C1292758 (UMLS CUI [1,1])
C0079611 (UMLS CUI [1,2])
C1517677 (UMLS CUI [2,1])
C0005957 (UMLS CUI [2,2])
Biospecimen Study T-Cell Receptor | Biospecimen Study Gene Expression Profile
Item
availability of biological material for the study of tcr and gene-profile;
boolean
C2347026 (UMLS CUI [1,1])
C2603343 (UMLS CUI [1,2])
C0034790 (UMLS CUI [1,3])
C2347026 (UMLS CUI [2,1])
C2603343 (UMLS CUI [2,2])
C1956267 (UMLS CUI [2,3])
Age
Item
age ≥ 15 years;
boolean
C0001779 (UMLS CUI [1])
Stages All
Item
all stages;
boolean
C1300072 (UMLS CUI [1,1])
C0444868 (UMLS CUI [1,2])
Bone marrow infiltration Percent
Item
infiltrated bone marrow <25%;
boolean
C3854434 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
Liver function | Renal function | Cardiac function | Exception Alteration Relationship Lymphoma
Item
normal liver, renal and cardiac functions, except for alterations directly related to lymphoma;
boolean
C0232741 (UMLS CUI [1])
C0232804 (UMLS CUI [2])
C0232164 (UMLS CUI [3])
C1705847 (UMLS CUI [4,1])
C1515926 (UMLS CUI [4,2])
C0439849 (UMLS CUI [4,3])
C0024299 (UMLS CUI [4,4])
Treatment Schedule Generation Last
Item
estimates of treatment according to one of the last generation schedules;
boolean
C0039798 (UMLS CUI [1,1])
C0040808 (UMLS CUI [1,2])
C0079411 (UMLS CUI [1,3])
C1517741 (UMLS CUI [1,4])
Informed Consent
Item
written informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hepatitis C | Hepatitis B surface antigen positive | HIV Infection
Item
patients with previous hcv, hbsag+ or suffering from hiv;
boolean
C0019196 (UMLS CUI [1])
C0149709 (UMLS CUI [2])
C0019693 (UMLS CUI [3])
Organic disease Independent of Lymphoma
Item
patients with organic pathology not related to lymphoma.
boolean
C0683324 (UMLS CUI [1,1])
C0332291 (UMLS CUI [1,2])
C0024299 (UMLS CUI [1,3])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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