ID

43538

Description

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

Mots-clés

Versions (3)
  1. 06/11/2016 06/11/2016 -
  2. 06/11/2016 06/11/2016 -
  3. 20/09/2021 20/09/2021 -
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20 septembre 2021

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Creative Commons BY-NC 3.0
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Pre-phase Therapy PETAL Study NCT00554164

Allemand Anglais

Pre-phase Therapy

1 Formulaires  
  1. StudyEvent: ODM
    1. Pre-phase Therapy
Patient demographics
Description

Patient demographics

Examination date
Description

Examination date

Type de données

date

Alias
UMLS CUI [1]
C2826643
Patient height
Description

Patient height

Type de données

float

Unités de mesure
  • cm
Alias
UMLS CUI [1]
C0489786
cm
Patient weight
Description

Patient weight

Type de données

float

Alias
UMLS CUI [1]
C0005910
Body surface
Description

Body surface

Type de données

float

Alias
UMLS CUI [1]
C0005902
Therapy
Description

Therapy

Date of Therapy
Description

Date of Therapy

Type de données

date

Alias
UMLS CUI [1]
C1707637
Duration of treatment
Description

Duration of treatment

Type de données

integer

Unités de mesure
  • Tage
Alias
UMLS CUI [1]
C0444921
Tage
Chemotherapy Regimen
Description

Chemotherapy Regimen

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

Prednison

Type de données

integer

Unités de mesure
  • mg
Alias
UMLS CUI [1]
C0032952
mg
Vincristin
Description

Vincristin

Type de données

integer

Unités de mesure
  • mg
Alias
UMLS CUI [1]
C0042679
mg
Intrathecal therapy
Description

Intrathecal therapy

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

MTX

Type de données

integer

Unités de mesure
  • mg
Alias
UMLS CUI [1]
C0025677
mg
MTX i.th. am
Description

MTX date of application

Type de données

date

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

Cytarabin

Type de données

integer

Unités de mesure
  • mg
Alias
UMLS CUI [1]
C0010711
mg
Cytarabin i.th. am
Description

Cytarabin

Type de données

date

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

Supportive therapy

Antibiotic Prophylaxis
Description

Antibiotic Prophylaxis

Type de données

boolean

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

Pre-operative antibiotic prophylaxis administered

Type de données

integer

Unités de mesure
  • Tage
Alias
UMLS CUI [1]
C2114165
Tage
Antibiotic therapy
Description

Antibiotic therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0338237
Antibiotic therapy duration
Description

Antibiotic therapy duration

Type de données

integer

Unités de mesure
  • Tage
Alias
UMLS CUI [1,1]
C0338237
UMLS CUI [1,2]
C0444921
Tage
Platelet function
Description

Platelet function

Type de données

boolean

Alias
UMLS CUI [1]
C1254881
Platelet concentrate
Description

Platelet concentrate

Type de données

integer

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

Red Blood Cell Transfusion

Type de données

boolean

Alias
UMLS CUI [1]
C0086252
Blood erythrocyte concentration
Description

Blood erythrocyte concentration

Type de données

integer

Alias
UMLS CUI [1]
C0522048
Erythropoetin
Description

Erythropoetin

Type de données

boolean

Alias
UMLS CUI [1]
C0014822
Erythropoetin, Dosage
Description

Erythropoetin, Dosage

Type de données

integer

Alias
UMLS CUI [1]
C0014822
Parenteral Nutrition
Description

Parenteral Nutrition

Type de données

boolean

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

Parenteral Nutrition, Total

Type de données

integer

Unités de mesure
  • Tage
Alias
UMLS CUI [1]
C0030548
Tage
Analgesics
Description

Analgesics

Type de données

boolean

Alias
UMLS CUI [1]
C0002771
Analgesics duration
Description

Analgesics duration

Type de données

integer

Unités de mesure
  • Tage
Alias
UMLS CUI [1,1]
C0002771
UMLS CUI [1,2]
C0444921
Tage
Other
Description

Other

Type de données

text

Alias
UMLS CUI [1]
C0205394
Administration of medication
Description

Administration of medication

Alias
UMLS CUI-1
C3469597
Outpatients
Description

Outpatients

Type de données

boolean

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

Duration of therapy outpatient

Type de données

integer

Unités de mesure
  • Tage
Alias
UMLS CUI [1,1]
C0029921
UMLS CUI [1,2]
C0444921
Tage
Stationary
Description

Stationary

Type de données

boolean

Alias
UMLS CUI [1]
C0439835
Stationary duration
Description

Stationary duration

Type de données

integer

Unités de mesure
  • Tage
Alias
UMLS CUI [1,1]
C0444921
UMLS CUI [1,2]
C0444921
Tage
Comorbidity at the therapy begin
Description

Comorbidity at the therapy begin

Number Comorbidity
Description

Number Comorbidity

Type de données

integer

Alias
UMLS CUI [1]
C0009488
Description Comorbidity
Description

Description Comorbidity

Type de données

text

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

Comorbidity length

Type de données

text

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

Medication duration

Alias
UMLS CUI-1
C2826814
Number of medication
Description

Number of medication

Type de données

integer

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

Medication Name

Type de données

text

Alias
UMLS CUI [1]
C2360065
Indication
Description

Indication

Type de données

text

Alias
UMLS CUI [1]
C3146298
Intercurrent disease
Description

Intercurrent disease

Alias
UMLS CUI-1
C0277557
Intercurrent disease
Description

Intercurrent disease

Type de données

boolean

Alias
UMLS CUI [1]
C0277557
Footer module
Description

Footer module

Comment
Description

Comment

Type de données

text

Alias
UMLS CUI [1]
C0947611
Date of processing
Description

Date of processing

Type de données

date

Alias
UMLS CUI [1]
C1709694
Signature clinical investigator
Description

Signature clinical investigator

Type de données

boolean

Alias
UMLS CUI [1]
C0008961
Retour au début de la page

Similar models

Pre-phase Therapy

1 Formulaires
  1. StudyEvent: ODM
    1. Pre-phase Therapy
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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