ID

18897

Description

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

Keywords

  1. 11/23/16 11/23/16 -
  2. 11/23/16 11/23/16 -
Uploaded on

November 23, 2016

DOI

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License

Creative Commons BY-NC 3.0

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End of study PETAL Study NCT00554164

End of study

  1. StudyEvent: ODM
    1. End of study
Comorbidity
Description

Comorbidity

Comorbidity number
Description

Comorbidity number

Data type

integer

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0750480
Comorbidity description
Description

Comorbidity description

Data type

text

Alias
UMLS CUI [1,1]
C0678257
UMLS CUI [1,2]
C0009488
Begin
Description

Begin

Data type

date

Alias
UMLS CUI [1]
C0808070
End
Description

End

Data type

date

Measurement units
  • °C
Alias
UMLS CUI [1]
C0806020
°C
Ongoing
Description

Ongoing

Data type

integer

Alias
UMLS CUI [1]
C0549178
Therapy
Description

Therapy

Data type

integer

Alias
UMLS CUI [1]
C0087111
Therapy begin
Description

Therapy begin

Data type

date

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0439659
Therapy end
Description

Therapy end

Data type

integer

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0444930
Therapy ongoing
Description

Therapy ongoing

Data type

integer

Alias
UMLS CUI [1,1]
C0549178
UMLS CUI [1,2]
C0039798
Discontinuation
Description

Discontinuation

Alias
UMLS CUI-1
C0457454
Death date
Description

Death date

Data type

date

Alias
UMLS CUI [1]
C1148348
Discontinuation date
Description

Discontinuation date

Data type

date

Alias
UMLS CUI [1,1]
C1444662
UMLS CUI [1,2]
C0011008
Time of premature discontinuation
Description

Time of premature discontinuation

Data type

integer

Alias
UMLS CUI [1,1]
C0457454
UMLS CUI [1,2]
C0040223
Reason for premature discontinuation of trial participation
Description

Reason for premature discontinuation of trial participation

Data type

integer

Alias
UMLS CUI [1,1]
C0457454
UMLS CUI [1,2]
C0392360
Adverse event
Description

Adverse event

Alias
UMLS CUI-1
C0877248
Adverse event number
Description

Adverse event number

Data type

integer

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0237753
Begin
Description

Begin

Data type

date

Alias
UMLS CUI [1]
C0808070
End
Description

End

Data type

date

Alias
UMLS CUI [1]
C0806020
Adverse event
Description

Adverse event

Data type

text

Alias
UMLS CUI [1]
C0877248
Adverse event frequency
Description

Adverse event frequency

Data type

integer

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0439603
Adverse Event: Severity
Description

Adverse Event: Severity

Data type

integer

Alias
UMLS CUI [1]
C1710066
Adverse Event Action Code
Description

Adverse Event Action Code

Data type

integer

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0441472
UMLS CUI [1,3]
C0805701
Correlation with trial procedure
Description

Correlation with trial procedure

Data type

integer

Alias
UMLS CUI [1]
C1707520
Result of adverse event
Description

Result of adverse event

Data type

integer

Alias
UMLS CUI [1]
C2985628
Footer module
Description

Footer module

Comment
Description

Comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Date of processing
Description

Date of processing

Data type

date

Alias
UMLS CUI [1]
C1709694
Signature clinical investigator
Description

Signature clinical investigator

Data type

boolean

Alias
UMLS CUI [1]
C0008961

Similar models

End of study

  1. StudyEvent: ODM
    1. End of study
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Comorbidity
Comorbidity number
Item
Comorbidity number
integer
C0009488 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Comorbidity description
Item
Comorbidity description
text
C0678257 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
Begin
Item
Begin
date
C0808070 (UMLS CUI [1])
End
Item
End
date
C0806020 (UMLS CUI [1])
Ongoing
Item
Ongoing
integer
C0549178 (UMLS CUI [1])
Therapy
Item
Therapy
integer
C0087111 (UMLS CUI [1])
Therapy begin
Item
Therapy begin
date
C0087111 (UMLS CUI [1,1])
C0439659 (UMLS CUI [1,2])
Therapy end
Item
Therapy end
integer
C0087111 (UMLS CUI [1,1])
C0444930 (UMLS CUI [1,2])
Therapy ongoing
Item
Therapy ongoing
integer
C0549178 (UMLS CUI [1,1])
C0039798 (UMLS CUI [1,2])
Item Group
Discontinuation
C0457454 (UMLS CUI-1)
Death date
Item
Death date
date
C1148348 (UMLS CUI [1])
Discontinuation date
Item
Discontinuation date
date
C1444662 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Time of premature discontinuation
integer
C0457454 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Code List
Time of premature discontinuation
CL Item
Prephase (1)
CL Item
Cycle (2)
C1302181 (UMLS CUI-1)
CL Item
Arm A, cycle (3)
C1522541 (UMLS CUI-1)
CL Item
Arm B, cycle (4)
C1522541 (UMLS CUI-1)
CL Item
DHAP, cycle (5)
C0057634 (UMLS CUI-1)
CL Item
ESHAP, cycle (6)
C0285858 (UMLS CUI-1)
CL Item
Follow-up (7)
C1522577 (UMLS CUI-1)
CL Item
BEAM-R, cycle (8)
Item
Reason for premature discontinuation of trial participation
integer
C0457454 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
Reason for premature discontinuation of trial participation
CL Item
unknown (1)
C0439673 (UMLS CUI-1)
CL Item
death (2)
C0011065 (UMLS CUI-1)
CL Item
Lymphoma aftermath (3)
C0024299 (UMLS CUI-1)
CL Item
disease progression  (4)
C0242656 (UMLS CUI-1)
CL Item
toxicity (5)
C0013221 (UMLS CUI-1)
CL Item
protocol violation (6)
C1709750 (UMLS CUI-1)
CL Item
non-compliance (7)
C0457432 (UMLS CUI-1)
CL Item
lost to follow-up (8)
C1302313 (UMLS CUI-1)
CL Item
patient wish (9)
C0747309 (UMLS CUI-1)
CL Item
Physician Decision (10)
C1709536 (UMLS CUI-1)
Item Group
Adverse event
C0877248 (UMLS CUI-1)
Adverse event number
Item
Adverse event number
integer
C0877248 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Begin
Item
Begin
date
C0808070 (UMLS CUI [1])
End
Item
End
date
C0806020 (UMLS CUI [1])
Adverse event
Item
Adverse event
text
C0877248 (UMLS CUI [1])
Item
Adverse event frequency
integer
C0877248 (UMLS CUI [1,1])
C0439603 (UMLS CUI [1,2])
Code List
Adverse event frequency
CL Item
Once (1)
CL Item
Twice (2)
CL Item
Ongoing (3)
Item
Adverse Event: Severity
integer
C1710066 (UMLS CUI [1])
Code List
Adverse Event: Severity
CL Item
Mild (Mild)
C2945599 (UMLS CUI-1)
CL Item
Moderate (Moderate)
C0205081 (UMLS CUI-1)
CL Item
Severe (Severe)
C0205082 (UMLS CUI-1)
CL Item
Life threatening (4)
C2826244 (UMLS CUI-1)
CL Item
Death (5)
C0011065 (UMLS CUI-1)
Item
Adverse Event Action Code
integer
C0877248 (UMLS CUI [1,1])
C0441472 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
Code List
Adverse Event Action Code
CL Item
Agent Withdrawn (1)
C2349954 (UMLS CUI-1)
CL Item
Agent Dose Reduced (2)
C0441610 (UMLS CUI-1)
CL Item
Agent Dose Increased (3)
C0442805 (UMLS CUI-1)
CL Item
Agent Dose Not Changed (4)
C0443172 (UMLS CUI-1)
CL Item
Unknown (5)
C0439673 (UMLS CUI-1)
CL Item
Not Applicable (6)
C1272460 (UMLS CUI-1)
Item
Correlation with trial procedure
integer
C1707520 (UMLS CUI [1])
Code List
Correlation with trial procedure
CL Item
definite (1)
CL Item
probable (2)
CL Item
possible (3)
CL Item
not likely (4)
CL Item
no correlation (5)
CL Item
can not be assessed (6)
Item
Result of adverse event
integer
C2985628 (UMLS CUI [1])
Code List
Result of adverse event
CL Item
Patient restored (1)
C0846605 (UMLS CUI-1)
CL Item
Ongoing (2)
C0549178 (UMLS CUI-1)
CL Item
permanent damage (3)
C3640792 (UMLS CUI-1)
CL Item
malformation (4)
C0302142 (UMLS CUI-1)
CL Item
death (5)
C0011065 (UMLS CUI-1)
CL Item
unknown (6)
C0439673 (UMLS CUI-1)
Item Group
Footer module
Comment
Item
Comment
text
C0947611 (UMLS CUI [1])
Date of processing
Item
Date of processing
date
C1709694 (UMLS CUI [1])
Signature clinical investigator
Item
Signature clinical investigator
boolean
C0008961 (UMLS CUI [1])

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