ID

30309

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT00882011

Nyckelord

Versioner (2)
  1. 2018-05-28 2018-05-28 -
  2. 2018-05-28 2018-05-28 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

28 maj 2018

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Lymphoblastic Lymphoma NCT00882011

Engelsk

Eligibility Lymphoblastic Lymphoma NCT00882011

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

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

Prior Therapy Absent | Exception Emergency treatment

Datatyp

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;
Beskrivning

Medical History Nodal mass

Datatyp

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;
Beskrivning

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

Datatyp

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;
Beskrivning

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

Datatyp

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;
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
all stages;
Beskrivning

Stages All

Datatyp

boolean

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

Bone marrow infiltration Percent

Datatyp

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;
Beskrivning

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

Datatyp

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;
Beskrivning

Treatment Schedule Generation Last

Datatyp

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.
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

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

Hepatitis C | Hepatitis B surface antigen positive | HIV Infection

Datatyp

boolean

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

Organic disease Independent of Lymphoma

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0683324
UMLS CUI [1,2]
C0332291
UMLS CUI [1,3]
C0024299
Tillbaka till toppen

Similar models

Eligibility Lymphoblastic Lymphoma NCT00882011

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

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