ID

5481

Description

CWS-2007-HR: A randomised phase-​III trial of the Cooperative Soft-​Tissue-​Study-​Group for localised high-​risk rhabdomyosarcoma and localised Rhabdomyosarcoma-​like Soft Tissue Sarcoma in children, adolescents, and young adults http://clinicaltrials.gov/show/NCT00876031 http://www.cws.olgahospital-stuttgart.de

Link

http://clinicaltrials.gov/show/NCT00876031

Keywords

  1. 8/6/14 8/6/14 - Martin Dugas
Uploaded on

August 6, 2014

DOI

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License

Creative Commons BY 4.0

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CWS-2007-HR B1 - Ein-_Ausschlusskriterien DRKS00003774

B1 - Ein-/Ausschlusskriterien

Anzeige Namen auf Formular
Description

Anzeige Namen auf Formular

Patient
Description

Dummy item in ItemGroup 'Display patient'

Data type

text

Einschlusskriterien
Description

Einschlusskriterien

Written informed consent available
Description

Einschlusskriterium Einverständnisserklärung liegt vor

Data type

integer

RMS or RMS-'like' soft tissue tumor
Description

Einschlusskriterium RMS oder -like Weichteiltumor nachgewiesen

Data type

integer

Age > 6 month and <21 years at the time of randomisation
Description

Einschlusskriterium Alter

Data type

integer

Assigned to the High- or Very High or RMS-'like' group
Description

Einschlusskriterium Stratifizierung

Data type

integer

No contraindication preventing treatment
Description

Einschlusskriterium keine Kontraindikation Chemotherapie

Data type

integer

No previous malignant tumors
Description

Einschluskriterium kein Zweittumor

Data type

integer

Multimodal primary treatment completed
Description

Einschlusskriterium Standardtherapie protokollgerecht beendet

Data type

integer

In remission
Description

Einschlusskriterium Remission

Data type

integer

Long-term follow-up possible
Description

Einschlusskriterium FUP

Data type

integer

Date of consent CWS-2007-HR
Description

Datum der Einverständniserklärung für CWS-07-HR

Data type

date

Ausschlusskriterien
Description

Ausschlusskriterien

Pregnant or lactating woman
Description

Ausschluss Schwangerschaft, Stillzeit

Data type

integer

Other medical condition precluding treatment
Description

Ausschluss Erkrankung

Data type

integer

Refusal to use effective contraception
Description

Ausschluss Weigerung Kontrazeption

Data type

integer

Similar models

B1 - Ein-/Ausschlusskriterien

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Dummy item in ItemGroup 'Display patient'
Item
Patient
text
Item
Written informed consent available
integer
Code List
Written informed consent available
CL Item
no (2)
CL Item
yes (1)
Item
RMS or RMS-'like' soft tissue tumor
integer
Code List
RMS or RMS-'like' soft tissue tumor
CL Item
no (2)
CL Item
yes (1)
Item
Age > 6 month and <21 years at the time of randomisation
integer
Code List
Age > 6 month and <21 years at the time of randomisation
CL Item
no (2)
CL Item
yes (1)
Item
Assigned to the High- or Very High or RMS-'like' group
integer
Code List
Assigned to the High- or Very High or RMS-'like' group
CL Item
no (2)
CL Item
yes (1)
Item
No contraindication preventing treatment
integer
Code List
No contraindication preventing treatment
CL Item
no (2)
CL Item
yes (1)
Item
No previous malignant tumors
integer
Code List
No previous malignant tumors
CL Item
no (2)
CL Item
yes (1)
Item
Multimodal primary treatment completed
integer
Code List
Multimodal primary treatment completed
CL Item
no (2)
CL Item
yes (1)
Item
In remission
integer
Code List
In remission
CL Item
no (2)
CL Item
yes (1)
Item
Long-term follow-up possible
integer
Code List
Long-term follow-up possible
CL Item
no (2)
CL Item
yes (1)
Datum der Einverständniserklärung für CWS-07-HR
Item
Date of consent CWS-2007-HR
date
Item
Pregnant or lactating woman
integer
Code List
Pregnant or lactating woman
CL Item
no (2)
CL Item
yes (1)
Item
Other medical condition precluding treatment
integer
Code List
Other medical condition precluding treatment
CL Item
no (2)
CL Item
yes (1)
Item
Refusal to use effective contraception
integer
Code List
Refusal to use effective contraception
CL Item
no (2)
CL Item
yes (1)

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