ID

17540

Description

Study part: Comorbidities at study end LeMLAR-Studie. Lenalidomide in conjunction with methotrexate, leucovorin, cytarabine and rituximab for the treatment of relapsed or refractory CD20-positive aggressive lymphomas: an open-label, multicenter phase I/II trial. Publication granted by Prof. Dührsen and provided by Claudia Ose, University clinic Essen, NCT01788189, Version 1.3-28.04.2013.doc.

Keywords

  1. 9/22/16 9/22/16 -
Uploaded on

September 22, 2016

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Comorbidities at study end LeMLAR-Studie Lymphoma NCT01788189

Comorbidities at study end

Begleiterkrankungen
Description

Begleiterkrankungen

Alias
UMLS CUI-1
C0009488
Begleiterkrankungen bei Studieneinschluss
Description

Comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
Datum
Description

Date

Data type

date

Alias
UMLS CUI [1]
C0011008
Patientenidentifikation
Description

Patient ID

Data type

integer

Alias
UMLS CUI [1]
C1269815
Vom Lymphom unabhängige Begleiterkrankung bei Studieneinschluss
Description

Comorbidity

Data type

text

Alias
UMLS CUI [1]
C0009488
Erstdiagnose (Jahr)
Description

first diagnosis

Data type

partialDate

Alias
UMLS CUI [1,1]
C0205265
UMLS CUI [1,2]
C0011900
Kommentare
Description

Comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Datum der Bearbeitung
Description

date

Data type

date

Alias
UMLS CUI [1]
C0011008
Name
Description

name

Data type

text

Alias
UMLS CUI [1]
C0027365
Unterschrift
Description

signature

Data type

text

Alias
UMLS CUI [1]
C1519316

Similar models

Comorbidities at study end

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Begleiterkrankungen
C0009488 (UMLS CUI-1)
Comorbidity
Item
Begleiterkrankungen bei Studieneinschluss
boolean
C0009488 (UMLS CUI [1])
Date
Item
Datum
date
C0011008 (UMLS CUI [1])
Patient ID
Item
Patientenidentifikation
integer
C1269815 (UMLS CUI [1])
Comorbidity
Item
Vom Lymphom unabhängige Begleiterkrankung bei Studieneinschluss
text
C0009488 (UMLS CUI [1])
first diagnosis
Item
Erstdiagnose (Jahr)
partialDate
C0205265 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
Comment
Item
Kommentare
text
C0947611 (UMLS CUI [1])
date
Item
Datum der Bearbeitung
date
C0011008 (UMLS CUI [1])
name
Item
Name
text
C0027365 (UMLS CUI [1])
signature
Item
Unterschrift
text
C1519316 (UMLS CUI [1])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

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