ID

43538

Description

Positronen-Emissionstomographie-gesteuerte Therapie aggressiver Non-Hodgkin-Lymphome (PETAL-Studie) Universitätsklinikum Essen (UK Essen) EudraCT-Nummer: 2006-001641-33 NCT00554164

Keywords

  1. 11/6/16 11/6/16 -
  2. 11/6/16 11/6/16 -
  3. 9/20/21 9/20/21 -
Uploaded on

September 20, 2021

DOI

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License

Creative Commons BY-NC 3.0

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Pre-phase Therapy PETAL Study NCT00554164

Pre-phase Therapy

  1. StudyEvent: ODM
    1. Pre-phase Therapy
Untersuchungsinformationen
Description

Untersuchungsinformationen

Untersuchungs-/Therapiedatum
Description

Examination date

Data type

date

Alias
UMLS CUI [1]
C2826643
Größe
Description

Patient height

Data type

float

Measurement units
  • cm
Alias
UMLS CUI [1]
C0489786
cm
Gewicht
Description

Patient weight

Data type

float

Alias
UMLS CUI [1]
C0005910
Körperoberfläche
Description

Body surface

Data type

float

Alias
UMLS CUI [1]
C0005902
Therapiezeiten
Description

Therapiezeiten

1. Tag der (Vorphase/Chemo)Therapie
Description

Date of Therapy

Data type

date

Alias
UMLS CUI [1]
C1707637
Dauer der Vorphase-Therapie
Description

Duration of treatment

Data type

integer

Measurement units
  • Tage
Alias
UMLS CUI [1]
C0444921
Tage
Dosierung der Chemotherapeutika in diesem Zyklus
Description

Dosierung der Chemotherapeutika in diesem Zyklus

Alias
UMLS CUI-1
C0392920
UMLS CUI-2
C0178602
Prednison
Description

Prednison

Data type

integer

Measurement units
  • mg
Alias
UMLS CUI [1]
C0032952
mg
Vincristin
Description

Vincristin

Data type

integer

Measurement units
  • mg
Alias
UMLS CUI [1]
C0042679
mg
Intrathekale Therapie
Description

Intrathekale Therapie

Alias
UMLS CUI-1
C1831734
MTX i.th., Dosis
Description

MTX

Data type

integer

Measurement units
  • mg
Alias
UMLS CUI [1]
C0025677
mg
MTX i.th. am
Description

MTX date of application

Data type

date

Alias
UMLS CUI [1,1]
C0025677
UMLS CUI [1,2]
C0011008
Cytarabin i.th., Dosis
Description

Cytarabin

Data type

integer

Measurement units
  • mg
Alias
UMLS CUI [1]
C0010711
mg
Cytarabin i.th. am
Description

Cytarabin

Data type

date

Alias
UMLS CUI [1,1]
C0010711
UMLS CUI [1,2]
C0011008
Supportivtherapie
Description

Supportivtherapie

Antibiotika-Prophylaxe
Description

Antibiotic Prophylaxis

Data type

boolean

Alias
UMLS CUI [1]
C0282638
Antibiotika-Prophylaxe, Anzahl Tage
Description

Pre-operative antibiotic prophylaxis administered

Data type

integer

Measurement units
  • Tage
Alias
UMLS CUI [1]
C2114165
Tage
Antibiotika-Therapie
Description

Antibiotic therapy

Data type

boolean

Alias
UMLS CUI [1]
C0338237
Antibiotika-Therapie, Anzahl Tage
Description

Antibiotic therapy duration

Data type

integer

Measurement units
  • Tage
Alias
UMLS CUI [1,1]
C0338237
UMLS CUI [1,2]
C0444921
Tage
Thrombozyten-Transfusion
Description

Platelet function

Data type

boolean

Alias
UMLS CUI [1]
C1254881
Anzahl Konz.
Description

Platelet concentrate

Data type

integer

Alias
UMLS CUI [1]
C1294041
Erythrozyten-Transfusion
Description

Red Blood Cell Transfusion

Data type

boolean

Alias
UMLS CUI [1]
C0086252
Anzahl Ery Konz.
Description

Blood erythrocyte concentration

Data type

integer

Alias
UMLS CUI [1]
C0522048
Erythropoetin
Description

Erythropoetin

Data type

boolean

Alias
UMLS CUI [1]
C0014822
Erythropoetin, Dosis
Description

Erythropoetin, Dosage

Data type

integer

Alias
UMLS CUI [1]
C0014822
Parenterale Ernährung
Description

Parenteral Nutrition

Data type

boolean

Alias
UMLS CUI [1]
C0030547
Pareenterale Therapie, Anzahl Tage
Description

Parenteral Nutrition, Total

Data type

integer

Measurement units
  • Tage
Alias
UMLS CUI [1]
C0030548
Tage
Analgetika (Mukositis)
Description

Analgesics

Data type

boolean

Alias
UMLS CUI [1]
C0002771
Analgetika (Mukositis) Anzahl Tage
Description

Analgesics duration

Data type

integer

Measurement units
  • Tage
Alias
UMLS CUI [1,1]
C0002771
UMLS CUI [1,2]
C0444921
Tage
Sonstiges, was?
Description

Other

Data type

text

Alias
UMLS CUI [1]
C0205394
Ort der Verabreichung
Description

Ort der Verabreichung

Alias
UMLS CUI-1
C3469597
Ambulant
Description

Outpatients

Data type

boolean

Alias
UMLS CUI [1]
C0029921
Anz. Tage Ambulant
Description

Duration of therapy outpatient

Data type

integer

Measurement units
  • Tage
Alias
UMLS CUI [1,1]
C0029921
UMLS CUI [1,2]
C0444921
Tage
Stationär
Description

Stationary

Data type

boolean

Alias
UMLS CUI [1]
C0439835
Anz. Tage Stationär
Description

Stationary duration

Data type

integer

Measurement units
  • Tage
Alias
UMLS CUI [1,1]
C0444921
UMLS CUI [1,2]
C0444921
Tage
Komorbidität bei Therapiebeginn
Description

Komorbidität bei Therapiebeginn

Nr. Komorbidität
Description

Number Comorbidity

Data type

integer

Alias
UMLS CUI [1]
C0009488
Beschreibung Begleiterkrankung
Description

Description Comorbidity

Data type

text

Alias
UMLS CUI [1,1]
C0678257
UMLS CUI [1,2]
C0009488
Komorbidität seit
Description

Comorbidity length

Data type

text

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0872146
Dauermedikation bei Therapiebeginn
Description

Dauermedikation bei Therapiebeginn

Alias
UMLS CUI-1
C2826814
Nr. der Medikation
Description

Number of medication

Data type

integer

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0449788
Name der Medikation
Description

Medication Name

Data type

text

Alias
UMLS CUI [1]
C2360065
Indikation
Description

Indication

Data type

text

Alias
UMLS CUI [1]
C3146298
Interkurrente Erkrankung
Description

Interkurrente Erkrankung

Alias
UMLS CUI-1
C0277557
Interkurrente Erkrankung?
Description

Intercurrent disease

Data type

boolean

Alias
UMLS CUI [1]
C0277557
Arzt Datum und Unterschrift
Description

Arzt Datum und Unterschrift

Weiteres Vorgehen - Kommentar
Description

Comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Datum der Bearbeitung
Description

Date of processing

Data type

date

Alias
UMLS CUI [1]
C1709694
Unterschrift Prüfarzt (vorhanden?)
Description

Signature clinical investigator

Data type

boolean

Alias
UMLS CUI [1]
C0008961

Similar models

Pre-phase Therapy

  1. StudyEvent: ODM
    1. Pre-phase Therapy
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Untersuchungsinformationen
Examination date
Item
Untersuchungs-/Therapiedatum
date
C2826643 (UMLS CUI [1])
Patient height
Item
Größe
float
C0489786 (UMLS CUI [1])
Patient weight
Item
Gewicht
float
C0005910 (UMLS CUI [1])
Body surface
Item
Körperoberfläche
float
C0005902 (UMLS CUI [1])
Item Group
Therapiezeiten
Date of Therapy
Item
1. Tag der (Vorphase/Chemo)Therapie
date
C1707637 (UMLS CUI [1])
Duration of treatment
Item
Dauer der Vorphase-Therapie
integer
C0444921 (UMLS CUI [1])
Item Group
Dosierung der Chemotherapeutika in diesem Zyklus
C0392920 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
Prednison
Item
Prednison
integer
C0032952 (UMLS CUI [1])
Vincristin
Item
Vincristin
integer
C0042679 (UMLS CUI [1])
Item Group
Intrathekale Therapie
C1831734 (UMLS CUI-1)
MTX
Item
MTX i.th., Dosis
integer
C0025677 (UMLS CUI [1])
MTX date of application
Item
MTX i.th. am
date
C0025677 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Cytarabin
Item
Cytarabin i.th., Dosis
integer
C0010711 (UMLS CUI [1])
Cytarabin
Item
Cytarabin i.th. am
date
C0010711 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Supportivtherapie
Antibiotic Prophylaxis
Item
Antibiotika-Prophylaxe
boolean
C0282638 (UMLS CUI [1])
Pre-operative antibiotic prophylaxis administered
Item
Antibiotika-Prophylaxe, Anzahl Tage
integer
C2114165 (UMLS CUI [1])
Antibiotic therapy
Item
Antibiotika-Therapie
boolean
C0338237 (UMLS CUI [1])
Antibiotic therapy duration
Item
Antibiotika-Therapie, Anzahl Tage
integer
C0338237 (UMLS CUI [1,1])
C0444921 (UMLS CUI [1,2])
Platelet function
Item
Thrombozyten-Transfusion
boolean
C1254881 (UMLS CUI [1])
Platelet concentrate
Item
Anzahl Konz.
integer
C1294041 (UMLS CUI [1])
Red Blood Cell Transfusion
Item
Erythrozyten-Transfusion
boolean
C0086252 (UMLS CUI [1])
Blood erythrocyte concentration
Item
Anzahl Ery Konz.
integer
C0522048 (UMLS CUI [1])
Erythropoetin
Item
Erythropoetin
boolean
C0014822 (UMLS CUI [1])
Erythropoetin, Dosage
Item
Erythropoetin, Dosis
integer
C0014822 (UMLS CUI [1])
Parenteral Nutrition
Item
Parenterale Ernährung
boolean
C0030547 (UMLS CUI [1])
Parenteral Nutrition, Total
Item
Pareenterale Therapie, Anzahl Tage
integer
C0030548 (UMLS CUI [1])
Analgesics
Item
Analgetika (Mukositis)
boolean
C0002771 (UMLS CUI [1])
Analgesics duration
Item
Analgetika (Mukositis) Anzahl Tage
integer
C0002771 (UMLS CUI [1,1])
C0444921 (UMLS CUI [1,2])
Other
Item
Sonstiges, was?
text
C0205394 (UMLS CUI [1])
Item Group
Ort der Verabreichung
C3469597 (UMLS CUI-1)
Outpatients
Item
Ambulant
boolean
C0029921 (UMLS CUI [1])
Duration of therapy outpatient
Item
Anz. Tage Ambulant
integer
C0029921 (UMLS CUI [1,1])
C0444921 (UMLS CUI [1,2])
Stationary
Item
Stationär
boolean
C0439835 (UMLS CUI [1])
Stationary duration
Item
Anz. Tage Stationär
integer
C0444921 (UMLS CUI [1,1])
C0444921 (UMLS CUI [1,2])
Item Group
Komorbidität bei Therapiebeginn
Number Comorbidity
Item
Nr. Komorbidität
integer
C0009488 (UMLS CUI [1])
Description Comorbidity
Item
Beschreibung Begleiterkrankung
text
C0678257 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
Comorbidity length
Item
Komorbidität seit
text
C0009488 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Item Group
Dauermedikation bei Therapiebeginn
C2826814 (UMLS CUI-1)
Number of medication
Item
Nr. der Medikation
integer
C0013227 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Medication Name
Item
Name der Medikation
text
C2360065 (UMLS CUI [1])
Indication
Item
Indikation
text
C3146298 (UMLS CUI [1])
Item Group
Interkurrente Erkrankung
C0277557 (UMLS CUI-1)
Intercurrent disease
Item
Interkurrente Erkrankung?
boolean
C0277557 (UMLS CUI [1])
Item Group
Arzt Datum und Unterschrift
Comment
Item
Weiteres Vorgehen - Kommentar
text
C0947611 (UMLS CUI [1])
Date of processing
Item
Datum der Bearbeitung
date
C1709694 (UMLS CUI [1])
Signature clinical investigator
Item
Unterschrift Prüfarzt (vorhanden?)
boolean
C0008961 (UMLS CUI [1])

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