ID

32434

Beschrijving

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

Trefwoorden

Versies (5)
  1. 25-04-17 25-04-17 -
  2. 25-04-17 25-04-17 -
  3. 03-05-17 03-05-17 -
  4. 19-05-17 19-05-17 -
  5. 01-11-18 01-11-18 - Sarah Riepenhausen
Houder van rechten

German Hodgkin Study Group

Geüploaded op

1 november 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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German Hodgkin Study Group Study HD16/HD17/HD18 Chemotherapy regimen G6C DRKS00003455

Duits

Deutsche Hodgkin Studiengruppe: G6C Chemotherapiebogen

1 Formulieren  
Formularkopf
Beschrijving

Formularkopf

Alias
UMLS CUI-1
C1320722
Stempel des einsendenden Instituts
Beschrijving

Stamp of participating institution

Datatype

text

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

Phone number of participating institution

Datatype

integer

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

Address of responsible study center

Datatype

text

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

Patient Name

Datatype

text

Alias
UMLS CUI [1]
C1299487
Geburtsname
Beschrijving

Patient birth name

Datatype

text

Alias
UMLS CUI [1]
C1549652
Geburtsdatum
Beschrijving

Birth Date

Datatype

date

Alias
UMLS CUI [1]
C0421451
Adresse des Patienten
Beschrijving

Patient address

Datatype

text

Alias
UMLS CUI [1]
C0421449
Studien ID
Beschrijving

Study ID

Datatype

integer

Alias
UMLS CUI [1]
C2826693
Bogen ID
Beschrijving

CRF Indentificator

Datatype

integer

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

Case ID

Datatype

integer

Alias
UMLS CUI [1,1]
C1698493
UMLS CUI [1,2]
C0600091
Chemotherapiebogen
Beschrijving

Chemotherapiebogen

Alias
UMLS CUI-1
C0392920
Vorphase mit Dexamethason
Beschrijving

Nur vor Kurs 1: 4 Tage à 40mg

Datatype

boolean

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

Cycle Number

Datatype

integer

Alias
UMLS CUI [1]
C2045829
Erster Therapietag
Beschrijving

Treatment start date

Datatype

date

Alias
UMLS CUI [1]
C3173309
Letzter Therapietag
Beschrijving

Treatment End date

Datatype

date

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

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

Datatype

integer

Maateenheden
  • mg
Alias
UMLS CUI [1,1]
C0393022
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Cyclophosphamid Gesamtdosis in mg/Zyklus (Zyklus angeben)
Beschrijving

1250mg/m2 i.v Tag 1

Datatype

integer

Maateenheden
  • mg
Alias
UMLS CUI [1,1]
C0010583
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Adriamycin Gesamtdosis in mg/Zyklus (Zyklus angeben)
Beschrijving

35mg/m2 i.v Tag 1

Datatype

integer

Maateenheden
  • mg
Alias
UMLS CUI [1,1]
C0085752
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Etoposid/Etopophos. Gesamtdosis in mg/Zyklus
Beschrijving

200mg/m2 i.v Tag 1-3

Datatype

integer

Maateenheden
  • mg
Alias
UMLS CUI [1,1]
C0904036
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Procarbazin Gesamtdosis in mg/Zyklus
Beschrijving

100mg/m2 p.o Tag 1-7

Datatype

integer

Maateenheden
  • mg
Alias
UMLS CUI [1,1]
C0033223
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Prednison Gesamtdosis in mg/Zyklus
Beschrijving

40mg/m2 p.o Tag 1-14

Datatype

integer

Maateenheden
  • mg
Alias
UMLS CUI [1,1]
C0032952
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Vincristin Gesamtdosis in mg/Zyklus
Beschrijving

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

Datatype

integer

Maateenheden
  • mg
Alias
UMLS CUI [1,1]
C0042679
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
Bleomycin Gesamtdosis in mg/Zyklus
Beschrijving

10mg/m2 i.v Tag 8

Datatype

integer

Maateenheden
  • mg
Alias
UMLS CUI [1,1]
C1589326
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1302181
mg
G-CSF verabreicht
Beschrijving

GCSF

Datatype

boolean

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

GCSF number of days

Datatype

integer

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

Neupogen

Datatype

boolean

Alias
UMLS CUI [1]
C0733468
Neulasta
Beschrijving

Neulasta

Datatype

boolean

Alias
UMLS CUI [1]
C1171279
Granocyte
Beschrijving

Granocyte

Datatype

boolean

Alias
UMLS CUI [1]
C0218640
Andere GCSF
Beschrijving

Other GCSF

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079459
UMLS CUI [1,2]
C0205394
Erythropoetin
Beschrijving

Erythropoetin

Datatype

boolean

Alias
UMLS CUI [1]
C0014822
Falls Erythropoetin: Anzahl
Beschrijving

Erythropoetin, Count of Doses

Datatype

integer

Alias
UMLS CUI [1,1]
C0014822
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0750480
Thrombozytenkonzentrat
Beschrijving

Platelet Concentrate

Datatype

boolean

Alias
UMLS CUI [1]
C1293886
Falls Thrombozytenkonzentrat: Anzahl
Beschrijving

Count of Platelet Concentrates

Datatype

integer

Alias
UMLS CUI [1,1]
C1293886
UMLS CUI [1,2]
C0449788
Erythrozytenkonzentrat
Beschrijving

Red blood cell concentrate

Datatype

boolean

Alias
UMLS CUI [1]
C0086252
Falls Erythrozytenkonzentrate: Anzahl
Beschrijving

Count of Red blood cell concentrates

Datatype

integer

Alias
UMLS CUI [1,1]
C0086252
UMLS CUI [1,2]
C0449788
Febrile Neutropenie
Beschrijving

Febrile Neutropenia

Datatype

boolean

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

Days of inpatient care because of febrile neutropenia

Datatype

integer

Maateenheden
  • Tage
Alias
UMLS CUI [1,1]
C0449238
UMLS CUI [1,2]
C0019993
UMLS CUI [1,3]
C0746883
Tage
Leukos < 1000
Beschrijving

Leukopenia

Datatype

boolean

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

Days of Leukopenia

Datatype

integer

Maateenheden
  • Tage
Alias
UMLS CUI [1,1]
C0023530
UMLS CUI [1,2]
C0449238
Tage
Davon Tage mit Fieber größer oder gleich 38°C
Beschrijving

Days with fever equal or higher 38°C

Datatype

integer

Maateenheden
  • Tage
Alias
UMLS CUI [1,1]
C1959900
UMLS CUI [1,2]
C0449238
Tage
Labor vor Therapiebeginn
Beschrijving

Labor vor Therapiebeginn

Alias
UMLS CUI-1
C0022877
UMLS CUI-2
C0332152
UMLS CUI-3
C3173309
Kurs-Nr.
Beschrijving

Chemotherapy cycle

Datatype

integer

Alias
UMLS CUI [1]
C2045829
Hämoglobin
Beschrijving

Hemoglobin

Datatype

float

Maateenheden
  • g/dL
Alias
UMLS CUI [1]
C0019046
g/dL
Hämoglobin
Beschrijving

Hemoglobin

Datatype

float

Maateenheden
  • mmol/l
Alias
UMLS CUI [1]
C0019046
mmol/l
Leukozyten
Beschrijving

WBC

Datatype

float

Maateenheden
  • x10^3/µl
Alias
UMLS CUI [1]
C0023508
x10^3/µl
Thrombozyten
Beschrijving

Platelets

Datatype

integer

Maateenheden
  • x10^3/µl
Alias
UMLS CUI [1]
C0005821
x10^3/µl
Toxizitäten
Beschrijving

Toxizitäten

Kurs Nummer
Beschrijving

Cycle number

Datatype

integer

Alias
UMLS CUI [1]
C2045829
Systemische Therapie Nebenwirkungen CTC Grad 3/4
Beschrijving

Bei Toxizitäten CTC Grad 3/4 bitte volständig dokumentieren

Datatype

boolean

Alias
UMLS CUI [1,1]
C1516728
UMLS CUI [1,2]
C1883256
Anämie
Beschrijving

Anemia

Datatype

integer

Alias
UMLS CUI [1]
C0002871
Thrombopenie
Beschrijving

Thrombocytopenia

Datatype

integer

Alias
UMLS CUI [1]
C0040034
Leukopenie
Beschrijving

Leukopenia

Datatype

integer

Alias
UMLS CUI [1]
C0023530
Übelkeit/Erbrechen
Beschrijving

Nausea/Vomiting

Datatype

integer

Alias
UMLS CUI [1]
C0027498
Mukositis
Beschrijving

Mucositis

Datatype

integer

Alias
UMLS CUI [1]
C0038362
Verdauungstrakt
Beschrijving

Intestines

Datatype

integer

Alias
UMLS CUI [1]
C0021853
Urogenitaltrakt
Beschrijving

Genitourinary system

Datatype

integer

Alias
UMLS CUI [1]
C0042066
Respirationstrakt
Beschrijving

Respiratory system

Datatype

integer

Alias
UMLS CUI [1]
C0035237
Medikam. Fieber
Beschrijving

Fever, drug induced

Datatype

integer

Alias
UMLS CUI [1]
C2830448
Allergie
Beschrijving

Hypersensitivity

Datatype

integer

Alias
UMLS CUI [1]
C0020517
Herz
Beschrijving

Heart

Datatype

integer

Alias
UMLS CUI [1]
C0018787
Infektion
Beschrijving

Infection

Datatype

integer

Alias
UMLS CUI [1]
C0009450
Haut
Beschrijving

Skin

Datatype

integer

Alias
UMLS CUI [1]
C1123023
Nerven
Beschrijving

Nervous system

Datatype

integer

Alias
UMLS CUI [1]
C1269560
Therapieänderungen
Beschrijving

Therapieänderungen

Gab es jeweils in einem der beiden Kurse eine Änderung?
Beschrijving

Treatment changes during one of two cycles

Datatype

boolean

Alias
UMLS CUI [1]
C3665894
Dosisreduktion
Beschrijving

Dose reduction

Datatype

boolean

Alias
UMLS CUI [1]
C1707814
Therapieverzögerung
Beschrijving

>14 Tage

Datatype

boolean

Alias
UMLS CUI [1]
C1299700
Abbruch
Beschrijving

bei Abbruch bitte Abbruchbogen ausfüllen

Datatype

boolean

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

If discontinued, reason

Datatype

text

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

Progressive Disease

Datatype

boolean

Alias
UMLS CUI [1]
C1335499
Toxizität
Beschrijving

Toxicity

Datatype

boolean

Alias
UMLS CUI [1]
C0013221
Patientenwunsch
Beschrijving

Patient wish

Datatype

boolean

Alias
UMLS CUI [1]
C0747309
HL unabhängige Erkrankung
Beschrijving

Other condition than Hodgkin lymphoma

Datatype

boolean

Alias
UMLS CUI [1,1]
C2707304
UMLS CUI [1,2]
C0332300
UMLS CUI [1,3]
C0019829
Wenn ja, welche?
Beschrijving

If other condition, please specify

Datatype

text

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

Comments

Datatype

text

Alias
UMLS CUI [1]
C0947611
Datum
Beschrijving

Date of completion

Datatype

date

Alias
UMLS CUI [1]
C0011008
Unterschrift
Beschrijving

Signature

Datatype

text

Alias
UMLS CUI [1]
C1519316
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Similar models

Deutsche Hodgkin Studiengruppe: G6C Chemotherapiebogen

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
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
C0392920 (UMLS CUI-1)
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])
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])
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])
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])
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])
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])
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])
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])
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])
Erythropoetin
Item
Erythropoetin
boolean
C0014822 (UMLS CUI [1])
Erythropoetin, Count of Doses
Item
Falls Erythropoetin: Anzahl
integer
C0014822 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,3])
Platelet Concentrate
Item
Thrombozytenkonzentrat
boolean
C1293886 (UMLS CUI [1])
Count of Platelet Concentrates
Item
Falls Thrombozytenkonzentrat: Anzahl
integer
C1293886 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Red blood cell concentrate
Item
Erythrozytenkonzentrat
boolean
C0086252 (UMLS CUI [1])
Count of Red blood cell concentrates
Item
Falls Erythrozytenkonzentrate: Anzahl
integer
C0086252 (UMLS CUI [1,1])
C0449788 (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
C0449238 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
C0746883 (UMLS CUI [1,3])
Leukopenia
Item
Leukos < 1000
boolean
C0023530 (UMLS CUI [1])
Days of Leukopenia
Item
Anzahl der Tage Leukos < 1000
integer
C0023530 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Days with fever equal or higher 38°C
Item
Davon Tage mit Fieber größer oder gleich 38°C
integer
C1959900 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Item Group
Labor vor Therapiebeginn
C0022877 (UMLS CUI-1)
C0332152 (UMLS CUI-2)
C3173309 (UMLS CUI-3)
Chemotherapy cycle
Item
Kurs-Nr.
integer
C2045829 (UMLS CUI [1])
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
Cycle number
Item
Kurs Nummer
integer
C2045829 (UMLS CUI [1])
CTC Grade 3/4
Item
Systemische Therapie Nebenwirkungen CTC Grad 3/4
boolean
C1516728 (UMLS CUI [1,1])
C1883256 (UMLS CUI [1,2])
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 Änderung?
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])
C0332300 (UMLS CUI [1,2])
C0019829 (UMLS CUI [1,3])
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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