ID

18991

Beschrijving

Positronen-Emissionstomographie-gesteuerte Therapie aggressiver Non-Hodgkin-Lymphome (PETAL-Studie) Universitätsklinikum Essen (UK Essen) EudraCT-Nummer: 2006-001641-33 NCT00554164

Trefwoorden

  1. 30-10-16 30-10-16 -
  2. 28-11-16 28-11-16 -
Geüploaded op

28 november 2016

DOI

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Licentie

Creative Commons BY-NC 3.0

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Basic documentation PETAL Study NCT00554164

Basic documentation

  1. StudyEvent: ODM
    1. Basic documentation
Patient identification
Beschrijving

Patient identification

Alias
UMLS CUI-1
C1269815
Date of birth
Beschrijving

Date of birth

Datatype

date

Alias
UMLS CUI [1]
C0421451
Gender
Beschrijving

Gender

Datatype

integer

Alias
UMLS CUI [1]
C0079399
Histopathology finding
Beschrijving

Histopathology finding

Datatype

integer

Alias
UMLS CUI [1]
C0428093
Date of diagnosis
Beschrijving

Date of diagnosis

Datatype

date

Alias
UMLS CUI [1]
C2316983
CD20 Expressing Cell Measurement
Beschrijving

CD20 Expressing Cell Measurement

Datatype

boolean

Alias
UMLS CUI [1]
C3540684
International Prognostic Index
Beschrijving

International Prognostic Index

Datatype

integer

Alias
UMLS CUI [1]
C1512894
Pathology
Beschrijving

Pathology

Medical pathologist
Beschrijving

Medical pathologist

Datatype

integer

Alias
UMLS CUI [1]
C0334866
Histology #
Beschrijving

Histology #

Datatype

integer

Alias
UMLS CUI [1,1]
C0019638
UMLS CUI [1,2]
C0449788
Health care facility
Beschrijving

Health care facility

Datatype

text

Alias
UMLS CUI [1]
C0018704
Address
Beschrijving

Address

Datatype

text

Alias
UMLS CUI [1]
C0421449
Medical pathologist
Beschrijving

Medical pathologist

Datatype

integer

Alias
UMLS CUI [1]
C0334866
Nuclear Medicine Department
Beschrijving

Nuclear Medicine Department

Datatype

text

Alias
UMLS CUI [1]
C0028583
Inclusion and exclusion criteria
Beschrijving

Inclusion and exclusion criteria

Datatype

boolean

Alias
UMLS CUI [1]
C2826675
Inclusion/ Exclsuion critera not correct? Which criteria has not been met?
Beschrijving

Inclusion/ Exclsuion critera not correct? Which criteria has not been met?

Datatype

text

Alias
UMLS CUI [1]
C2827031
Date of start of treatment or therapy pre-phase
Beschrijving

Date of start of treatment or therapy pre-phase

Datatype

date

Alias
UMLS CUI [1,1]
C3173309
UMLS CUI [1,2]
C1548998
Date of start of CHOP regimen
Beschrijving

Date of start of CHOP regimen

Datatype

date

Alias
UMLS CUI [1,1]
C3173309
UMLS CUI [1,2]
C0163868
Footer module
Beschrijving

Footer module

Signature Clinical Investigator
Beschrijving

Signature Clinical Investigator

Datatype

boolean

Alias
UMLS CUI [1]
C0008961
Processing date
Beschrijving

Processing date

Datatype

date

Alias
UMLS CUI [1,1]
C1709694
UMLS CUI [1,2]
C0011008

Similar models

Basic documentation

  1. StudyEvent: ODM
    1. Basic documentation
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Patient identification
C1269815 (UMLS CUI-1)
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Item
Gender
integer
C0079399 (UMLS CUI [1])
Code List
Gender
CL Item
male (1)
CL Item
female (2)
Histopathology finding
Item
Histopathology finding
integer
C0428093 (UMLS CUI [1])
Date of diagnosis
Item
Date of diagnosis
date
C2316983 (UMLS CUI [1])
CD20 Expressing Cell Measurement
Item
CD20 Expressing Cell Measurement
boolean
C3540684 (UMLS CUI [1])
Item
International Prognostic Index
integer
C1512894 (UMLS CUI [1])
Code List
International Prognostic Index
CL Item
low (1)
CL Item
low-intermediate  (2)
CL Item
high-intermediate  (3)
CL Item
high (4)
Item Group
Pathology
Medical pathologist
Item
Medical pathologist
integer
C0334866 (UMLS CUI [1])
Histology #
Item
Histology #
integer
C0019638 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Health care facility
Item
Health care facility
text
C0018704 (UMLS CUI [1])
Address
Item
Address
text
C0421449 (UMLS CUI [1])
Item
Medical pathologist
integer
C0334866 (UMLS CUI [1])
Code List
Medical pathologist
Item
Nuclear Medicine Department
text
C0028583 (UMLS CUI [1])
Code List
Nuclear Medicine Department
CL Item
Berlin (P01)
CL Item
Dresden (P02)
CL Item
Essen (P03)
CL Item
Fulda (P04)
CL Item
Heidelberg (P05)
CL Item
München (P06)
CL Item
Münster, (P07)
CL Item
Bremen (P08)
CL Item
Hannover (P09)
CL Item
Paderborn (P10)
CL Item
Minden (P11)
CL Item
Kiel (P12)
CL Item
Leipzig (P13)
CL Item
Potsdam (P14)
CL Item
Stuttgart, (P15)
CL Item
Passau (P16)
CL Item
Regensburg (P17)
CL Item
Jülich (P18)
CL Item
Mönchengladbach (P19)
CL Item
Lüdenscheid (P20)
CL Item
Koblenz (P21)
CL Item
Aachen (P22)
CL Item
Jena (P23)
Inclusion and exclusion criteria
Item
Inclusion and exclusion criteria
boolean
C2826675 (UMLS CUI [1])
Inclusion/ Exclsuion critera not correct? Which criteria has not been met?
Item
Inclusion/ Exclsuion critera not correct? Which criteria has not been met?
text
C2827031 (UMLS CUI [1])
Date of start of treatment or therapy pre-phase
Item
Date of start of treatment or therapy pre-phase
date
C3173309 (UMLS CUI [1,1])
C1548998 (UMLS CUI [1,2])
Date of start of CHOP regimen
Item
Date of start of CHOP regimen
date
C3173309 (UMLS CUI [1,1])
C0163868 (UMLS CUI [1,2])
Item Group
Footer module
Signature Clinical Investigator
Item
Signature Clinical Investigator
boolean
C0008961 (UMLS CUI [1])
Processing date
Item
Processing date
date
C1709694 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])

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