ID

21512

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 (5)
  1. 25/4/17 25/4/17 -
  2. 25/4/17 25/4/17 -
  3. 3/5/17 3/5/17 -
  4. 19/5/17 19/5/17 -
  5. 1/11/18 1/11/18 - Sarah Riepenhausen
Subido en

25 de abril de 2017

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
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German Hodgkin Study Group Study HD16/HD17/HD18 Chemotherapy regimen G6C

Alemán

Deutsche Hodgkin Studiengruppe: G6C Chemotherapiebogen

1 formularios  
Formularkopf
Descripción

Formularkopf

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

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
Chemotherapiebogen
Descripción

Chemotherapiebogen

Vorphase mit Dexamethason
Descripción

Nur vor Kurs 1: 4 Tage à 40mg

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0011777
UMLS CUI [1,2]
C1880049
Kurs-Nr.
Descripción

Cycle Number

Tipo de datos

integer

Alias
UMLS CUI [1]
C2045829
Erster Therapietag
Descripción

Treatment start date

Tipo de datos

date

Alias
UMLS CUI [1]
C3173309
Letzter Therapietag
Descripción

Treatment End date

Tipo de datos

date

Alias
UMLS CUI [1]
C1531784
Rituximab Gesamtdosis in mg/Zyklus
Descripción

375mg/m2 i.v im 4.Zyklus Tag 0+3; ab 5.Zyklus Tag 1

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C0393022
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Rituximab Zyklus Nr.
Descripción

Rituximab cycle number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C0393022
Cyclophosphamid Gesamtdosis in mg/Zyklus (Zyklus angeben)
Descripción

1250mg/m2 i.v Tag 1

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C0010583
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Cyclophosphamid Zyklus Nr.
Descripción

Cyclophosphamide cycle number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C0010583
Adriamycin Gesamtdosis in mg/Zyklus (Zyklus angeben)
Descripción

35mg/m2 i.v Tag 1

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C0085752
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Adriamycin Zyklus Nr.
Descripción

Adriamycin cycle number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C0085752
Etoposid/Etopophos. Gesamtdosis in mg/Zyklus
Descripción

200mg/m2 i.v Tag 1-3

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C0904036
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Etoposid/EtopophosZyklus Nr.
Descripción

Etoposide/Etopophos cycle number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C0904036
Procarbazin Gesamtdosis in mg/Zyklus
Descripción

100mg/m2 p.o Tag 1-7

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C0033223
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Procarbazin Zyklus Nr.
Descripción

Procarbazine cycle number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C0033223
Prednison Gesamtdosis in mg/Zyklus
Descripción

40mg/m2 p.o Tag 1-14

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C0032952
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Prednison Zyklus Nr.
Descripción

Prednisone cycle number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C0032952
Vincristin Gesamtdosis in mg/Zyklus
Descripción

1,4mg/m2 i.v (max. 2mg) Tag 8

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C0042679
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Vincristin Zyklus Nr.
Descripción

Vincristine cycle number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C0042679
Bleomycin Gesamtdosis in mg/Zyklus
Descripción

10mg/m2 i.v Tag 8

Tipo de datos

integer

Unidades de medida
  • mg
Alias
UMLS CUI [1,1]
C1589326
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Bleomycin Zyklus Nr.
Descripción

Bleomycine cycle number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C1589326
G-CSF verabreicht
Descripción

GCSF

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0376562
G-CSF Tage
Descripción

GCSF number of days

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0376562
UMLS CUI [1,2]
C0556971
Neupogen
Descripción

Neupogen

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0733468
Neulasta
Descripción

Neulasta

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1171279
Granocyte
Descripción

Granocyte

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0218640
Andere GCSF
Descripción

Other GCSF

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0079459
UMLS CUI [1,2]
C0205394
Febrile Neutropenie
Descripción

Febrile Neutropenia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0746883
Tage stationär wg. febriler Neutropenie
Descripción

Days of inpatient care because of febrile neutropenia

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0746883
Leukos < 1000
Descripción

Leukopenia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023530
Anzahl der Tage Leukos < 1000
Descripción

Days of Leukopenia

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0023530
UMLS CUI [1,2]
C0556971
Anzahl Tage mit Fieber größer oder gleich 38°C
Descripción

Days with fever equal or higher 38°C

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1959900
UMLS CUI [1,2]
C0556971
Labor vor Therapiebeginn
Descripción

Labor vor Therapiebeginn

Hämoglobin
Descripción

Hemoglobin

Tipo de datos

float

Unidades de medida
  • g/dL
Alias
UMLS CUI [1]
C0019046
g/dL
Hämoglobin
Descripción

Hemoglobin

Tipo de datos

float

Unidades de medida
  • mmol/l
Alias
UMLS CUI [1]
C0019046
mmol/l
Leukozyten
Descripción

WBC

Tipo de datos

float

Unidades de medida
  • x10^3/µl
Alias
UMLS CUI [1]
C0023508
x10^3/µl
Thrombozyten
Descripción

Platelets

Tipo de datos

integer

Unidades de medida
  • x10^3/µl
Alias
UMLS CUI [1]
C0005821
x10^3/µl
Toxizitäten
Descripción

Toxizitäten

Systemische Therapie Nebenwirkungen CTC Grad 3/4
Descripción

Bei Toxizitäten CTC Grad 3/4 bitte volständig dokumentieren

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1706735
Kurs Nummer
Descripción

Cycle number

Tipo de datos

integer

Alias
UMLS CUI [1]
C2045829
Anämie
Descripción

Anemia

Tipo de datos

integer

Alias
UMLS CUI [1]
C0002871
Thrombopenie
Descripción

Thrombocytopenia

Tipo de datos

integer

Alias
UMLS CUI [1]
C0040034
Leukopenie
Descripción

Leukopenia

Tipo de datos

integer

Alias
UMLS CUI [1]
C0023530
Übelkeit/Erbrechen
Descripción

Nausea/Vomiting

Tipo de datos

integer

Alias
UMLS CUI [1]
C0027498
Mukositis
Descripción

Mucositis

Tipo de datos

integer

Alias
UMLS CUI [1]
C0038362
Verdauungstrakt
Descripción

Intestines

Tipo de datos

integer

Alias
UMLS CUI [1]
C0021853
Urogenitaltrakt
Descripción

Genitourinary system

Tipo de datos

integer

Alias
UMLS CUI [1]
C0042066
Respirationstrakt
Descripción

Respiratory system

Tipo de datos

integer

Alias
UMLS CUI [1]
C0035237
Medikam. Fieber
Descripción

Fever, drug induced

Tipo de datos

integer

Alias
UMLS CUI [1]
C2830448
Allergie
Descripción

Hypersensitivity

Tipo de datos

integer

Alias
UMLS CUI [1]
C0020517
Herz
Descripción

Heart

Tipo de datos

integer

Alias
UMLS CUI [1]
C0018787
Infektion
Descripción

Infection

Tipo de datos

integer

Alias
UMLS CUI [1]
C0009450
Haut
Descripción

Skin

Tipo de datos

integer

Alias
UMLS CUI [1]
C1123023
Nerven
Descripción

Nervous system

Tipo de datos

integer

Alias
UMLS CUI [1]
C1269560
Therapieänderungen
Descripción

Therapieänderungen

Gab es jeweils in einem der beiden Kurse eine Anderung?
Descripción

Treatment changes during one of two cycles

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3665894
Dosisreduktion
Descripción

Dose reduction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1707814
Therapieverzögerung
Descripción

>14 Tage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1299700
Abbruch
Descripción

bei Abbruch bitte Abbruchbogen ausfüllen

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0457454
Falls ja, Begründung
Descripción

If discontinued, reason

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0566251
UMLS CUI [1,2]
C0457454
Progreß unter Therapie
Descripción

Progressive Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1335499
Toxizität
Descripción

Toxicity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013221
Patientenwunsch
Descripción

Patient wish

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0747309
HL unabhängige Erkrankung
Descripción

Other condition than Hodgkin lymphoma

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2707304
UMLS CUI [1,2]
C0019829
Wenn ja, welche?
Descripción

If other condition, please specify

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2707304
UMLS CUI [1,2]
C1521902
Bemerkungen
Descripción

Comments

Tipo de datos

text

Alias
UMLS CUI [1]
C0947611
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: G6C Chemotherapiebogen

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Formularkopf
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
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
Chemotherapiebogen
Pre-cycle with dexamethasone
Item
Vorphase mit Dexamethason
boolean
C0011777 (UMLS CUI [1,1])
C1880049 (UMLS CUI [1,2])
Cycle Number
Item
Kurs-Nr.
integer
C2045829 (UMLS CUI [1])
Treatment start date
Item
Erster Therapietag
date
C3173309 (UMLS CUI [1])
Treatment End date
Item
Letzter Therapietag
date
C1531784 (UMLS CUI [1])
Rituximab total dose per cycle
Item
Rituximab Gesamtdosis in mg/Zyklus
integer
C0393022 (UMLS CUI [1,1])
C2986497 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
Rituximab cycle number
Item
Rituximab Zyklus Nr.
integer
C1302181 (UMLS CUI [1,1])
C0393022 (UMLS CUI [1,2])
Cyclophosphamide total dose per cycle
Item
Cyclophosphamid Gesamtdosis in mg/Zyklus (Zyklus angeben)
integer
C0010583 (UMLS CUI [1,1])
C2986497 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
Cyclophosphamide cycle number
Item
Cyclophosphamid Zyklus Nr.
integer
C1302181 (UMLS CUI [1,1])
C0010583 (UMLS CUI [1,2])
Adriamycin total dose per cycle
Item
Adriamycin Gesamtdosis in mg/Zyklus (Zyklus angeben)
integer
C0085752 (UMLS CUI [1,1])
C2986497 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
Adriamycin cycle number
Item
Adriamycin Zyklus Nr.
integer
C1302181 (UMLS CUI [1,1])
C0085752 (UMLS CUI [1,2])
Etoposide/Etopophos. total dose per cycle
Item
Etoposid/Etopophos. Gesamtdosis in mg/Zyklus
integer
C0904036 (UMLS CUI [1,1])
C2986497 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
Etoposide/Etopophos cycle number
Item
Etoposid/EtopophosZyklus Nr.
integer
C1302181 (UMLS CUI [1,1])
C0904036 (UMLS CUI [1,2])
Procarbazine total dose per cycle
Item
Procarbazin Gesamtdosis in mg/Zyklus
integer
C0033223 (UMLS CUI [1,1])
C2986497 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
Procarbazine cycle number
Item
Procarbazin Zyklus Nr.
integer
C1302181 (UMLS CUI [1,1])
C0033223 (UMLS CUI [1,2])
Prednisone total dose per cycle
Item
Prednison Gesamtdosis in mg/Zyklus
integer
C0032952 (UMLS CUI [1,1])
C2986497 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
Prednisone cycle number
Item
Prednison Zyklus Nr.
integer
C1302181 (UMLS CUI [1,1])
C0032952 (UMLS CUI [1,2])
Vincristine total dose per cycle
Item
Vincristin Gesamtdosis in mg/Zyklus
integer
C0042679 (UMLS CUI [1,1])
C2986497 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
Vincristine cycle number
Item
Vincristin Zyklus Nr.
integer
C1302181 (UMLS CUI [1,1])
C0042679 (UMLS CUI [1,2])
Bleomycine total dose per cycle
Item
Bleomycin Gesamtdosis in mg/Zyklus
integer
C1589326 (UMLS CUI [1,1])
C2986497 (UMLS CUI [1,2])
C1302181 (UMLS CUI [1,3])
Bleomycine cycle number
Item
Bleomycin Zyklus Nr.
integer
C1302181 (UMLS CUI [1,1])
C1589326 (UMLS CUI [1,2])
GCSF
Item
G-CSF verabreicht
boolean
C0376562 (UMLS CUI [1])
GCSF number of days
Item
G-CSF Tage
integer
C0376562 (UMLS CUI [1,1])
C0556971 (UMLS CUI [1,2])
Neupogen
Item
Neupogen
boolean
C0733468 (UMLS CUI [1])
Neulasta
Item
Neulasta
boolean
C1171279 (UMLS CUI [1])
Granocyte
Item
Granocyte
boolean
C0218640 (UMLS CUI [1])
Other GCSF
Item
Andere GCSF
boolean
C0079459 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Febrile Neutropenia
Item
Febrile Neutropenie
boolean
C0746883 (UMLS CUI [1])
Days of inpatient care because of febrile neutropenia
Item
Tage stationär wg. febriler Neutropenie
integer
C0019993 (UMLS CUI [1,1])
C0746883 (UMLS CUI [1,2])
Leukopenia
Item
Leukos < 1000
boolean
C0023530 (UMLS CUI [1])
Days of Leukopenia
Item
Anzahl der Tage Leukos < 1000
integer
C0023530 (UMLS CUI [1,1])
C0556971 (UMLS CUI [1,2])
Days with fever equal or higher 38°C
Item
Anzahl Tage mit Fieber größer oder gleich 38°C
integer
C1959900 (UMLS CUI [1,1])
C0556971 (UMLS CUI [1,2])
Item Group
Labor vor Therapiebeginn
Hemoglobin
Item
Hämoglobin
float
C0019046 (UMLS CUI [1])
Hemoglobin
Item
Hämoglobin
float
C0019046 (UMLS CUI [1])
WBC
Item
Leukozyten
float
C0023508 (UMLS CUI [1])
Platelets
Item
Thrombozyten
integer
C0005821 (UMLS CUI [1])
Item Group
Toxizitäten
CTC Grade 3/4
Item
Systemische Therapie Nebenwirkungen CTC Grad 3/4
boolean
C1706735 (UMLS CUI [1])
Cycle number
Item
Kurs Nummer
integer
C2045829 (UMLS CUI [1])
Item
Anämie
integer
C0002871 (UMLS CUI [1])
Anemia
Code List
Anämie
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Thrombopenie
integer
C0040034 (UMLS CUI [1])
Anemia
Code List
Thrombopenie
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Leukopenie
integer
C0023530 (UMLS CUI [1])
Anemia
Code List
Leukopenie
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Übelkeit/Erbrechen
integer
C0027498 (UMLS CUI [1])
Anemia
Code List
Übelkeit/Erbrechen
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Mukositis
integer
C0038362 (UMLS CUI [1])
Anemia
Code List
Mukositis
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Verdauungstrakt
integer
C0021853 (UMLS CUI [1])
Anemia
Code List
Verdauungstrakt
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Urogenitaltrakt
integer
C0042066 (UMLS CUI [1])
Anemia
Code List
Urogenitaltrakt
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Respirationstrakt
integer
C0035237 (UMLS CUI [1])
Anemia
Code List
Respirationstrakt
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Medikam. Fieber
integer
C2830448 (UMLS CUI [1])
Anemia
Code List
Medikam. Fieber
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Allergie
integer
C0020517 (UMLS CUI [1])
Anemia
Code List
Allergie
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Herz
integer
C0018787 (UMLS CUI [1])
Anemia
Code List
Herz
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Infektion
integer
C0009450 (UMLS CUI [1])
Anemia
Code List
Infektion
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Haut
integer
C1123023 (UMLS CUI [1])
Anemia
Code List
Haut
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item
Nerven
integer
C1269560 (UMLS CUI [1])
Anemia
Code List
Nerven
CL Item
CTC3 (1)
CL Item
CTC4 (2)
Item Group
Therapieänderungen
Treatment changes during one of two cycles
Item
Gab es jeweils in einem der beiden Kurse eine Anderung?
boolean
C3665894 (UMLS CUI [1])
Dose reduction
Item
Dosisreduktion
boolean
C1707814 (UMLS CUI [1])
Therapy delay
Item
Therapieverzögerung
boolean
C1299700 (UMLS CUI [1])
Discontinuation
Item
Abbruch
boolean
C0457454 (UMLS CUI [1])
If discontinued, reason
Item
Falls ja, Begründung
text
C0566251 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
Progressive Disease
Item
Progreß unter Therapie
boolean
C1335499 (UMLS CUI [1])
Toxicity
Item
Toxizität
boolean
C0013221 (UMLS CUI [1])
Patient wish
Item
Patientenwunsch
boolean
C0747309 (UMLS CUI [1])
Other condition than Hodgkin lymphoma
Item
HL unabhängige Erkrankung
boolean
C2707304 (UMLS CUI [1,1])
C0019829 (UMLS CUI [1,2])
If other condition, please specify
Item
Wenn ja, welche?
text
C2707304 (UMLS CUI [1,1])
C1521902 (UMLS CUI [1,2])
Comments
Item
Bemerkungen
text
C0947611 (UMLS CUI [1])
Date of completion
Item
Datum
date
C0011008 (UMLS CUI [1])
Signature
Item
Unterschrift
text
C1519316 (UMLS CUI [1])
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