ID

30309

Description

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

Keywords

Versions (2)
  1. 5/28/18 5/28/18 -
  2. 5/28/18 5/28/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 28, 2018

DOI

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License

Creative Commons BY-NC 3.0
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Eligibility Lymphoblastic Lymphoma NCT00882011

English

Eligibility Lymphoblastic Lymphoma NCT00882011

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

Prior Therapy Absent | Exception Emergency treatment

Data type

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;
Description

Medical History Nodal mass

Data type

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;
Description

T-cell lymphoblastic lymphoma Immunophenotyping | Bone Marrow Involvement Bone Marrow Examination | Lymph node sample Obtain Difficulty Bone Marrow Examination

Data type

boolean

Alias
UMLS CUI [1,1]
C1292758
UMLS CUI [1,2]
C0079611
UMLS CUI [2,1]
C1517677
UMLS CUI [2,2]
C0005957
UMLS CUI [3,1]
C0444261
UMLS CUI [3,2]
C1301820
UMLS CUI [3,3]
C0332218
UMLS CUI [3,4]
C0005957
availability of biological material for the study of tcr and gene-profile;
Description

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

Data type

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;
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
all stages;
Description

Stages All

Data type

boolean

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

Bone marrow infiltration Percent

Data type

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;
Description

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

Data type

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;
Description

Treatment Schedule Generation Last

Data type

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.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

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

Hepatitis C | Hepatitis B surface antigen positive | HIV Infection

Data type

boolean

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

Organic disease Independent of Lymphoma

Data type

boolean

Alias
UMLS CUI [1,1]
C0683324
UMLS CUI [1,2]
C0332291
UMLS CUI [1,3]
C0024299
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Similar models

Eligibility Lymphoblastic Lymphoma NCT00882011

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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 | Lymph node sample Obtain Difficulty 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])
C0444261 (UMLS CUI [3,1])
C1301820 (UMLS CUI [3,2])
C0332218 (UMLS CUI [3,3])
C0005957 (UMLS CUI [3,4])
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])
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