ID

43538

Beschreibung

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

Stichworte

Versionen (3)
  1. 06.11.16 06.11.16 -
  2. 06.11.16 06.11.16 -
  3. 20.09.21 20.09.21 -
Hochgeladen am

20. September 2021

DOI

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Pre-phase Therapy PETAL Study NCT00554164

Deutsch Englisch

Pre-phase Therapy

1 Formulare  
  1. StudyEvent: ODM
    1. Pre-phase Therapy
Patient demographics
Beschreibung

Patient demographics

Examination date
Beschreibung

Examination date

Datentyp

date

Alias
UMLS CUI [1]
C2826643
Patient height
Beschreibung

Patient height

Datentyp

float

Maßeinheiten
  • cm
Alias
UMLS CUI [1]
C0489786
cm
Patient weight
Beschreibung

Patient weight

Datentyp

float

Alias
UMLS CUI [1]
C0005910
Body surface
Beschreibung

Body surface

Datentyp

float

Alias
UMLS CUI [1]
C0005902
Therapy
Beschreibung

Therapy

Date of Therapy
Beschreibung

Date of Therapy

Datentyp

date

Alias
UMLS CUI [1]
C1707637
Duration of treatment
Beschreibung

Duration of treatment

Datentyp

integer

Maßeinheiten
  • Tage
Alias
UMLS CUI [1]
C0444921
Tage
Chemotherapy Regimen
Beschreibung

Chemotherapy Regimen

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

Prednison

Datentyp

integer

Maßeinheiten
  • mg
Alias
UMLS CUI [1]
C0032952
mg
Vincristin
Beschreibung

Vincristin

Datentyp

integer

Maßeinheiten
  • mg
Alias
UMLS CUI [1]
C0042679
mg
Intrathecal therapy
Beschreibung

Intrathecal therapy

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

MTX

Datentyp

integer

Maßeinheiten
  • mg
Alias
UMLS CUI [1]
C0025677
mg
MTX i.th. am
Beschreibung

MTX date of application

Datentyp

date

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

Cytarabin

Datentyp

integer

Maßeinheiten
  • mg
Alias
UMLS CUI [1]
C0010711
mg
Cytarabin i.th. am
Beschreibung

Cytarabin

Datentyp

date

Alias
UMLS CUI [1,1]
C0010711
UMLS CUI [1,2]
C0011008
Supportive therapy
Beschreibung

Supportive therapy

Antibiotic Prophylaxis
Beschreibung

Antibiotic Prophylaxis

Datentyp

boolean

Alias
UMLS CUI [1]
C0282638
Pre-operative antibiotic prophylaxis administered
Beschreibung

Pre-operative antibiotic prophylaxis administered

Datentyp

integer

Maßeinheiten
  • Tage
Alias
UMLS CUI [1]
C2114165
Tage
Antibiotic therapy
Beschreibung

Antibiotic therapy

Datentyp

boolean

Alias
UMLS CUI [1]
C0338237
Antibiotic therapy duration
Beschreibung

Antibiotic therapy duration

Datentyp

integer

Maßeinheiten
  • Tage
Alias
UMLS CUI [1,1]
C0338237
UMLS CUI [1,2]
C0444921
Tage
Platelet function
Beschreibung

Platelet function

Datentyp

boolean

Alias
UMLS CUI [1]
C1254881
Platelet concentrate
Beschreibung

Platelet concentrate

Datentyp

integer

Alias
UMLS CUI [1]
C1294041
Red Blood Cell Transfusion
Beschreibung

Red Blood Cell Transfusion

Datentyp

boolean

Alias
UMLS CUI [1]
C0086252
Blood erythrocyte concentration
Beschreibung

Blood erythrocyte concentration

Datentyp

integer

Alias
UMLS CUI [1]
C0522048
Erythropoetin
Beschreibung

Erythropoetin

Datentyp

boolean

Alias
UMLS CUI [1]
C0014822
Erythropoetin, Dosage
Beschreibung

Erythropoetin, Dosage

Datentyp

integer

Alias
UMLS CUI [1]
C0014822
Parenteral Nutrition
Beschreibung

Parenteral Nutrition

Datentyp

boolean

Alias
UMLS CUI [1]
C0030547
Parenteral Nutrition, Total
Beschreibung

Parenteral Nutrition, Total

Datentyp

integer

Maßeinheiten
  • Tage
Alias
UMLS CUI [1]
C0030548
Tage
Analgesics
Beschreibung

Analgesics

Datentyp

boolean

Alias
UMLS CUI [1]
C0002771
Analgesics duration
Beschreibung

Analgesics duration

Datentyp

integer

Maßeinheiten
  • Tage
Alias
UMLS CUI [1,1]
C0002771
UMLS CUI [1,2]
C0444921
Tage
Other
Beschreibung

Other

Datentyp

text

Alias
UMLS CUI [1]
C0205394
Administration of medication
Beschreibung

Administration of medication

Alias
UMLS CUI-1
C3469597
Outpatients
Beschreibung

Outpatients

Datentyp

boolean

Alias
UMLS CUI [1]
C0029921
Duration of therapy outpatient
Beschreibung

Duration of therapy outpatient

Datentyp

integer

Maßeinheiten
  • Tage
Alias
UMLS CUI [1,1]
C0029921
UMLS CUI [1,2]
C0444921
Tage
Stationary
Beschreibung

Stationary

Datentyp

boolean

Alias
UMLS CUI [1]
C0439835
Stationary duration
Beschreibung

Stationary duration

Datentyp

integer

Maßeinheiten
  • Tage
Alias
UMLS CUI [1,1]
C0444921
UMLS CUI [1,2]
C0444921
Tage
Comorbidity at the therapy begin
Beschreibung

Comorbidity at the therapy begin

Number Comorbidity
Beschreibung

Number Comorbidity

Datentyp

integer

Alias
UMLS CUI [1]
C0009488
Description Comorbidity
Beschreibung

Description Comorbidity

Datentyp

text

Alias
UMLS CUI [1,1]
C0678257
UMLS CUI [1,2]
C0009488
Comorbidity length
Beschreibung

Comorbidity length

Datentyp

text

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0872146
Medication duration
Beschreibung

Medication duration

Alias
UMLS CUI-1
C2826814
Number of medication
Beschreibung

Number of medication

Datentyp

integer

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0449788
Medication Name
Beschreibung

Medication Name

Datentyp

text

Alias
UMLS CUI [1]
C2360065
Indication
Beschreibung

Indication

Datentyp

text

Alias
UMLS CUI [1]
C3146298
Intercurrent disease
Beschreibung

Intercurrent disease

Alias
UMLS CUI-1
C0277557
Intercurrent disease
Beschreibung

Intercurrent disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0277557
Footer module
Beschreibung

Footer module

Comment
Beschreibung

Comment

Datentyp

text

Alias
UMLS CUI [1]
C0947611
Date of processing
Beschreibung

Date of processing

Datentyp

date

Alias
UMLS CUI [1]
C1709694
Signature clinical investigator
Beschreibung

Signature clinical investigator

Datentyp

boolean

Alias
UMLS CUI [1]
C0008961
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Pre-phase Therapy

1 Formulare
  1. StudyEvent: ODM
    1. Pre-phase Therapy
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Patient demographics
Examination date
Item
Examination date
date
C2826643 (UMLS CUI [1])
Patient height
Item
Patient height
float
C0489786 (UMLS CUI [1])
Patient weight
Item
Patient weight
float
C0005910 (UMLS CUI [1])
Body surface
Item
Body surface
float
C0005902 (UMLS CUI [1])
Item Group
Therapy
Date of Therapy
Item
Date of Therapy
date
C1707637 (UMLS CUI [1])
Duration of treatment
Item
Duration of treatment
integer
C0444921 (UMLS CUI [1])
Item Group
Chemotherapy Regimen
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
Intrathecal therapy
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
Supportive therapy
Antibiotic Prophylaxis
Item
Antibiotic Prophylaxis
boolean
C0282638 (UMLS CUI [1])
Pre-operative antibiotic prophylaxis administered
Item
Pre-operative antibiotic prophylaxis administered
integer
C2114165 (UMLS CUI [1])
Antibiotic therapy
Item
Antibiotic therapy
boolean
C0338237 (UMLS CUI [1])
Antibiotic therapy duration
Item
Antibiotic therapy duration
integer
C0338237 (UMLS CUI [1,1])
C0444921 (UMLS CUI [1,2])
Platelet function
Item
Platelet function
boolean
C1254881 (UMLS CUI [1])
Platelet concentrate
Item
Platelet concentrate
integer
C1294041 (UMLS CUI [1])
Red Blood Cell Transfusion
Item
Red Blood Cell Transfusion
boolean
C0086252 (UMLS CUI [1])
Blood erythrocyte concentration
Item
Blood erythrocyte concentration
integer
C0522048 (UMLS CUI [1])
Erythropoetin
Item
Erythropoetin
boolean
C0014822 (UMLS CUI [1])
Erythropoetin, Dosage
Item
Erythropoetin, Dosage
integer
C0014822 (UMLS CUI [1])
Parenteral Nutrition
Item
Parenteral Nutrition
boolean
C0030547 (UMLS CUI [1])
Parenteral Nutrition, Total
Item
Parenteral Nutrition, Total
integer
C0030548 (UMLS CUI [1])
Analgesics
Item
Analgesics
boolean
C0002771 (UMLS CUI [1])
Analgesics duration
Item
Analgesics duration
integer
C0002771 (UMLS CUI [1,1])
C0444921 (UMLS CUI [1,2])
Other
Item
Other
text
C0205394 (UMLS CUI [1])
Item Group
Administration of medication
C3469597 (UMLS CUI-1)
Outpatients
Item
Outpatients
boolean
C0029921 (UMLS CUI [1])
Duration of therapy outpatient
Item
Duration of therapy outpatient
integer
C0029921 (UMLS CUI [1,1])
C0444921 (UMLS CUI [1,2])
Stationary
Item
Stationary
boolean
C0439835 (UMLS CUI [1])
Stationary duration
Item
Stationary duration
integer
C0444921 (UMLS CUI [1,1])
C0444921 (UMLS CUI [1,2])
Item Group
Comorbidity at the therapy begin
Number Comorbidity
Item
Number Comorbidity
integer
C0009488 (UMLS CUI [1])
Description Comorbidity
Item
Description Comorbidity
text
C0678257 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
Comorbidity length
Item
Comorbidity length
text
C0009488 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Item Group
Medication duration
C2826814 (UMLS CUI-1)
Number of medication
Item
Number of medication
integer
C0013227 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Medication Name
Item
Medication Name
text
C2360065 (UMLS CUI [1])
Indication
Item
Indication
text
C3146298 (UMLS CUI [1])
Item Group
Intercurrent disease
C0277557 (UMLS CUI-1)
Intercurrent disease
Item
Intercurrent disease
boolean
C0277557 (UMLS CUI [1])
Item Group
Footer module
Comment
Item
Comment
text
C0947611 (UMLS CUI [1])
Date of processing
Item
Date of processing
date
C1709694 (UMLS CUI [1])
Signature clinical investigator
Item
Signature clinical investigator
boolean
C0008961 (UMLS CUI [1])
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