ID

32461

Descripción

HD16 NCT Nr.: NCT00736320 HD16 for Early Stages - Treatment Optimization Trial in the First-line Treatment of Early Stage Hodgkin Lymphoma; Treatment Stratification by Means of FDG-PET. This study is designed to test the non-inferiority of the experimental arm compared to the standard arm in terms of Progression free survival (PFS). HD17 NCT Nr.: NCT01356680 HD17 for Intermediate Stages - Treatment Optimization Trial in the First-Line Treatment of Intermediate Stage Hodgkin Lymphoma.This study is designed to test the non-inferiority of the experimental arm compared to the standard arm in terms of progression free survival (PFS). HD18 NCT Nr.: NCT00515554 HD18 for Advanced Stages in Hodgkins Lymphoma. This study is designed to test: in patients with negative positron-emission tomography (PET) after 2 cycles of BEACOPPesc chemotherapy: whether the number of cycles can be reduced without compromising progression free survival (PFS) (2 further cycles vs. 6 further cycles) for patients with positive PET after 2 cycles: whether intensifying BEACOPPesc chemotherapy by adding Rituximab improves PFS. Permission granted by: Andreas Engert, M.D. Chairman, German Hodgkin Study Group Professor for Internal Medicine Hematology & Oncology University Hospital of Cologne Department of Internal Medicine I Kerpener Str. 62 D-50924 Köln Phone: +49-221-478-5933/5966 Fax: +49-221-478-3778 a.engert@uni-koeln.de

Palabras clave

Versiones (3)
  1. 24/4/17 24/4/17 -
  2. 3/5/17 3/5/17 -
  3. 1/11/18 1/11/18 - Sarah Riepenhausen
Titular de derechos de autor

German Hodgkin Study Group

Subido en

1 de noviembre de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0
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German Hodgkin Study Group Study HD16/HD17/HD18 Final Report DRKS00003455 DRKS00003457

Alemán

Deutsche Hodgkin Studiengruppe: Abschlussbogen

1 formularios  
Formularkopf
Descripción

Formularkopf

Alias
UMLS CUI-1
C1320722
Stempel des einsendenden Instituts
Descripción

Stamp of participating institution

Tipo de datos

text

Alias
UMLS CUI [1]
C2347449
Telefonnummer des einsendenden Instituts (bitte mit Durchwahl)
Descripción

Phone number of participating institution

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2347449
UMLS CUI [1,2]
C1515258
Adresse der verantwortlichen Studienzentrale
Descripción

Address of responsible study center

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2825181
UMLS CUI [1,2]
C1442065
Patientenname
Descripción

Patient Name

Tipo de datos

text

Alias
UMLS CUI [1]
C1299487
Geburtsname
Descripción

Patient birth name

Tipo de datos

text

Alias
UMLS CUI [1]
C1549652
Geburtsdatum
Descripción

Birth Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0421451
Adresse des Patienten
Descripción

Patient address

Tipo de datos

text

Alias
UMLS CUI [1]
C0421449
Datum des histologischen Befundes
Descripción

Histology report date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0807321
UMLS CUI [1,2]
C011008
Studien ID
Descripción

Study ID

Tipo de datos

integer

Alias
UMLS CUI [1]
C2826693
Bogen ID
Descripción

CRF Indentificator

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1516308
UMLS CUI [1,2]
C0600091
Case ID
Descripción

Case ID

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1698493
UMLS CUI [1,2]
C0600091
Patient verstorben
Descripción

Patient verstorben

Alias
UMLS CUI-1
C0011065
UMLS CUI-2
C1516308
Todesdatum
Descripción

Date of Death

Tipo de datos

date

Alias
UMLS CUI [1]
C1148348
Todesursache
Descripción

Freitext s.u.

Tipo de datos

integer

Alias
UMLS CUI [1]
C0007465
Sektion durchgeführt
Descripción

Autopsy done

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004398
UMLS CUI [1,2]
C0884358
Sektion durchgeführt am
Descripción

Autopsy date

Tipo de datos

date

Alias
UMLS CUI [1]
C3864942
Sektionsergebnis
Descripción

Autopsy result

Tipo de datos

integer

Alias
UMLS CUI [1]
C0332145
Wo wurde der Tumor aufgefunden?
Descripción

Neoplasm found

Tipo de datos

text

Alias
UMLS CUI [1]
C0332145
Hat eine Sekundärneoplasie vorgelegen?
Descripción

Second primary

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0751623
Art der Sekundärneoplasie
Descripción

Second primary

Tipo de datos

integer

Alias
UMLS CUI [1]
C0751623
Diagnosedatum der Sekundärneoplasie
Descripción

Second primary date of diagnosis

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0751623
UMLS CUI [1,2]
C2316983
Detaillierte Information zur Todesursache
Descripción

Bitte Kopie des letzten Arztbriefes beifügen

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1533716
UMLS CUI [1,2]
C0007465
Datum
Descripción

Date of completion

Tipo de datos

date

Alias
UMLS CUI [1]
C0011008
Unterschrift
Descripción

Signature

Tipo de datos

text

Alias
UMLS CUI [1]
C1519316
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Similar models

Deutsche Hodgkin Studiengruppe: Abschlussbogen

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Formularkopf
C1320722 (UMLS CUI-1)
Stamp of participating institution
Item
Stempel des einsendenden Instituts
text
C2347449 (UMLS CUI [1])
Phone number of participating institution
Item
Telefonnummer des einsendenden Instituts (bitte mit Durchwahl)
integer
C2347449 (UMLS CUI [1,1])
C1515258 (UMLS CUI [1,2])
Address of responsible study center
Item
Adresse der verantwortlichen Studienzentrale
text
C2825181 (UMLS CUI [1,1])
C1442065 (UMLS CUI [1,2])
Patient Name
Item
Patientenname
text
C1299487 (UMLS CUI [1])
Patient birth name
Item
Geburtsname
text
C1549652 (UMLS CUI [1])
Birth Date
Item
Geburtsdatum
date
C0421451 (UMLS CUI [1])
Patient address
Item
Adresse des Patienten
text
C0421449 (UMLS CUI [1])
Histology report date
Item
Datum des histologischen Befundes
date
C0807321 (UMLS CUI [1,1])
C011008 (UMLS CUI [1,2])
Item
Studien ID
integer
C2826693 (UMLS CUI [1])
Study ID
Code List
Studien ID
CL Item
HD16 (1)
CL Item
HD17 (2)
CL Item
HD18 (3)
CRF Indentificator
Item
Bogen ID
integer
C1516308 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Case ID
Item
Case ID
integer
C1698493 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Item Group
Patient verstorben
C0011065 (UMLS CUI-1)
C1516308 (UMLS CUI-2)
Date of Death
Item
Todesdatum
date
C1148348 (UMLS CUI [1])
Item
Todesursache
integer
C0007465 (UMLS CUI [1])
Cause of death
Code List
Todesursache
CL Item
Tumorbedingt (1)
CL Item
Therapiebedingt (2)
CL Item
Sekundärneoplasie (3)
CL Item
Unfall (4)
CL Item
Suizid (5)
CL Item
Sonstige (6)
Autopsy done
Item
Sektion durchgeführt
boolean
C0004398 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
Autopsy date
Item
Sektion durchgeführt am
date
C3864942 (UMLS CUI [1])
Item
Sektionsergebnis
integer
C0332145 (UMLS CUI [1])
Autopsy result
Code List
Sektionsergebnis
CL Item
Tumor nicht auffindbar  (1)
CL Item
Tumor auffindbar (2)
Item
Wo wurde der Tumor aufgefunden?
text
C0332145 (UMLS CUI [1])
Autopsy result
Code List
Wo wurde der Tumor aufgefunden?
Second primary
Item
Hat eine Sekundärneoplasie vorgelegen?
boolean
C0751623 (UMLS CUI [1])
Item
Art der Sekundärneoplasie
integer
C0751623 (UMLS CUI [1])
Second primary
Code List
Art der Sekundärneoplasie
CL Item
Leukämie,MDS (1)
CL Item
NHL (2)
CL Item
Solider Tumor (3)
Second primary date of diagnosis
Item
Diagnosedatum der Sekundärneoplasie
date
C0751623 (UMLS CUI [1,1])
C2316983 (UMLS CUI [1,2])
Detailed information cause of death
Item
Detaillierte Information zur Todesursache
text
C1533716 (UMLS CUI [1,1])
C0007465 (UMLS CUI [1,2])
Date of completion
Item
Datum
date
C0011008 (UMLS CUI [1])
Signature
Item
Unterschrift
text
C1519316 (UMLS CUI [1])
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