ID

43554

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. 11/8/16 11/8/16 -
  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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CHOP chemotherapy regimen PETAL Study NCT00554164

CHOP chemotherapy regimen

Patient demographics
Description

Patient demographics

Examination date
Description

Treatment date

Data type

date

Alias
UMLS CUI [1]
C3173309
Patient height
Description

Patient height

Data type

float

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

Patient weight

Data type

float

Alias
UMLS CUI [1]
C0005910
Body surface
Description

Body surface

Data type

float

Alias
UMLS CUI [1]
C0005902
CHOP cycle number
Description

CHOP cycle number

Data type

integer

Alias
UMLS CUI [1,1]
C0055598
UMLS CUI [1,2]
C1302181
Therapy
Description

Therapy

Date of Therapy
Description

Date of Therapy

Data type

date

Alias
UMLS CUI [1]
C1707637
Rituximab
Description

Rituximab

Data type

date

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0393022
UMLS CUI [1,2]
C1316946
days
Chemotherapy Regimen
Description

Chemotherapy Regimen

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
Rituximab
Description

Rituximab

Data type

integer

Measurement units
  • mg
Alias
UMLS CUI [1]
C0393022
mg
Doxorubicin
Description

Doxorubicin

Data type

integer

Measurement units
  • mg
Alias
UMLS CUI [1]
C0013089
mg
Cyclophosphamid
Description

Cyclophosphamid

Data type

integer

Measurement units
  • mg
Alias
UMLS CUI [1]
C0010583
mg
Intrathecal therapy
Description

Intrathecal therapy

Alias
UMLS CUI-1
C1831734
MTX
Description

MTX

Data type

integer

Measurement units
  • mg
Alias
UMLS CUI [1]
C0025677
mg
MTX date of application
Description

MTX date of application

Data type

date

Alias
UMLS CUI [1,1]
C0025677
UMLS CUI [1,2]
C0011008
Cytarabin
Description

Cytarabin

Data type

integer

Measurement units
  • mg
Alias
UMLS CUI [1]
C0010711
mg
Cytarabin date
Description

Cytarabin date

Data type

date

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

Supportive therapy

Antibiotic Prophylaxis
Description

Antibiotic Prophylaxis

Data type

boolean

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

Pre-operative antibiotic prophylaxis administered

Data type

integer

Measurement units
  • days
Alias
UMLS CUI [1]
C2114165
days
Antibiotic therapy
Description

Antibiotic therapy

Data type

boolean

Alias
UMLS CUI [1]
C0338237
Antibiotic therapy duration
Description

Antibiotic therapy duration

Data type

integer

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0338237
UMLS CUI [1,2]
C0444921
days
Platelet function
Description

Platelet function

Data type

boolean

Alias
UMLS CUI [1]
C1254881
Platelet concentrate
Description

Platelet concentrate

Data type

integer

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

Red Blood Cell Transfusion

Data type

boolean

Alias
UMLS CUI [1]
C0086252
Blood erythrocyte concentration
Description

Blood erythrocyte concentration

Data type

integer

Alias
UMLS CUI [1]
C0522048
Erythropoetin
Description

Erythropoetin

Data type

boolean

Alias
UMLS CUI [1]
C0014822
Erythropoetin, Dosage
Description

Erythropoetin, Dosage

Data type

integer

Alias
UMLS CUI [1]
C0014822
Parenteral Nutrition
Description

Parenteral Nutrition

Data type

boolean

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

Parenteral Nutrition, Total

Data type

integer

Measurement units
  • days
Alias
UMLS CUI [1]
C0030548
days
Analgesics
Description

Analgesics

Data type

boolean

Alias
UMLS CUI [1]
C0002771
Analgesics duration
Description

Analgesics duration

Data type

integer

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0002771
UMLS CUI [1,2]
C0444921
days
Other
Description

Other

Data type

text

Alias
UMLS CUI [1]
C0205394
Administration of medication
Description

Administration of medication

Alias
UMLS CUI-1
C3469597
Outpatients
Description

Outpatients

Data type

boolean

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

Duration of therapy outpatient

Data type

integer

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0029921
UMLS CUI [1,2]
C0444921
days
Stationary
Description

Stationary

Data type

boolean

Alias
UMLS CUI [1]
C0439835
Stationary duration
Description

Stationary duration

Data type

integer

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0444921
UMLS CUI [1,2]
C0444921
days
Comorbidity at the therapy begin
Description

Comorbidity at the therapy begin

Number Comorbidity
Description

Number Comorbidity

Data type

integer

Alias
UMLS CUI [1]
C0009488
Description Comorbidity
Description

Description Comorbidity

Data type

text

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

Comorbidity length

Data type

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

Data type

integer

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

Medication Name

Data type

text

Alias
UMLS CUI [1]
C2360065
Indication
Description

Indication

Data type

text

Alias
UMLS CUI [1]
C3146298
G-CSF
Description

G-CSF

Alias
UMLS CUI-1
C0796404
G-CSF?
Description

G-CSF?

Data type

boolean

Alias
UMLS CUI [1]
C0079459
PEG-Filgrastim date
Description

PEG-Filgrastim date

Data type

date

Alias
UMLS CUI [1,1]
C0210630
UMLS CUI [1,2]
C0011008
Filgrastim dosage
Description

Filgrastim dosage

Data type

integer

Measurement units
  • μg tgl.
Alias
UMLS CUI [1,1]
C0210630
UMLS CUI [1,2]
C0178602
μg tgl.
Filgrastim Duration of treatment
Description

Filgrastim Duration of treatment

Data type

integer

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0210630
UMLS CUI [1,2]
C0444921
days
Cycle duration
Description

Cycle duration

Interval
Description

Interval

Data type

integer

Alias
UMLS CUI [1]
C1272706
Reason for prolonged interval
Description

Reason for prolonged interval

Data type

integer

Alias
UMLS CUI [1]
C1272706
Therapy discontinuation
Description

Therapy discontinuation

Therapy discontinuation
Description

Therapy discontinuation

Data type

boolean

Alias
UMLS CUI [1]
C0677162
Progressive Disease
Description

Progressive Disease

Data type

boolean

Alias
UMLS CUI [1]
C1335499
Drug toxicity
Description

Drug toxicity

Data type

boolean

Alias
UMLS CUI [1]
C0013221
Patient wish
Description

Patient wish

Data type

boolean

Alias
UMLS CUI [1]
C0747309
Other
Description

Other

Data type

boolean

Alias
UMLS CUI [1]
C0205394
Stem Cell Mobilization
Description

Stem Cell Mobilization

Stem Cell Mobilization
Description

Stem Cell Mobilization

Data type

boolean

Alias
UMLS CUI [1]
C0524864
CD34 stem cell count procedure
Description

CD34 stem cell count procedure

Data type

integer

Measurement units
  • pro kg KG
Alias
UMLS CUI [1]
C1277788
pro kg KG
Lab results prior to chemotherapy cycle
Description

Lab results prior to chemotherapy cycle

Alias
UMLS CUI-1
C1302181
HB
Description

HB

Data type

float

Alias
UMLS CUI [1]
C0518015
Leucocytes
Description

Leucocytes

Data type

float

Alias
UMLS CUI [1]
C0023508
Granulocytes
Description

Granulocytes

Data type

float

Alias
UMLS CUI [1]
C0857490
Thrombocytes
Description

Thrombocytes

Data type

float

Alias
UMLS CUI [1]
C0005821
Creatinin
Description

Creatinin

Data type

float

Alias
UMLS CUI [1]
C0201976
Bilirubin
Description

Bilirubin

Data type

float

Alias
UMLS CUI [1]
C1278039
C-reactives Proteine
Description

C-reactives Proteine

Data type

float

Alias
UMLS CUI [1]
C0006560
Other
Description

Other

Data type

float

Lab results during interval after chemotherapy cycle
Description

Lab results during interval after chemotherapy cycle

Chemotherapy cycle
Description

Chemotherapy cycle

Data type

text

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C3468389
HB
Description

HB

Data type

float

Alias
UMLS CUI [1]
C0518015
Leucocytes
Description

Leucocytes

Data type

float

Alias
UMLS CUI [1]
C0023508
Granulocyte count
Description

Granulocyte count

Data type

float

Alias
UMLS CUI [1]
C0857490
Thrombozctes
Description

Thrombozctes

Data type

float

Alias
UMLS CUI [1]
C1287267
Toxicity
Description

Toxicity

Alias
UMLS CUI-1
C0013221
Creatinin
Description

Creatinin

Data type

integer

Alias
UMLS CUI [1]
C0201976
Nausea
Description

Nausea

Data type

float

Alias
UMLS CUI [1]
C0027497
Vomiting
Description

Vomiting

Data type

integer

Alias
UMLS CUI [1]
C0042963
Diarrhoe
Description

Diarrhoe

Data type

integer

Alias
UMLS CUI [1]
C0011991
Stomatitis
Description

Stomatitis

Data type

integer

Alias
UMLS CUI [1]
C0038362
Obstipation
Description

Obstipation

Data type

integer

Alias
UMLS CUI [1]
C1963087
Stomatitis
Description

Stomatitis

Data type

integer

Alias
UMLS CUI [1]
C0038362
Hemorrhagic cystitis
Description

Hemorrhagic cystitis

Data type

integer

Alias
UMLS CUI [1]
C0085692
Level of consciousness
Description

Level of consciousness

Data type

integer

Alias
UMLS CUI [1]
C0234425
Alopezie
Description

Alopezie

Data type

integer

Alias
UMLS CUI [1]
C1559115
Infection
Description

Infection

Data type

integer

Alias
UMLS CUI [1]
C0009450
Toxicity
Description

Toxicity

Data type

integer

Alias
UMLS CUI [1]
C0013221
Intercurrent disease
Description

Intercurrent disease

Alias
UMLS CUI-1
C0277557
Intercurrent disease
Description

Intercurrent disease

Data type

boolean

Alias
UMLS CUI [1]
C0277557
Footer module
Description

Footer module

Comment
Description

Comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Date of processing
Description

Date of processing

Data type

date

Alias
UMLS CUI [1]
C1709694
Signature clinical investigator
Description

Signature clinical investigator

Data type

boolean

Alias
UMLS CUI [1]
C0008961

Similar models

CHOP chemotherapy regimen

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Patient demographics
Treatment date
Item
Examination date
date
C3173309 (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])
CHOP cycle number
Item
CHOP cycle number
integer
C0055598 (UMLS CUI [1,1])
C1302181 (UMLS CUI [1,2])
Item Group
Therapy
Date of Therapy
Item
Date of Therapy
date
C1707637 (UMLS CUI [1])
Rituximab
Item
Rituximab
date
C0393022 (UMLS CUI [1,1])
C1316946 (UMLS CUI [1,2])
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])
Rituximab
Item
Rituximab
integer
C0393022 (UMLS CUI [1])
Doxorubicin
Item
Doxorubicin
integer
C0013089 (UMLS CUI [1])
Cyclophosphamid
Item
Cyclophosphamid
integer
C0010583 (UMLS CUI [1])
Item Group
Intrathecal therapy
C1831734 (UMLS CUI-1)
MTX
Item
MTX
integer
C0025677 (UMLS CUI [1])
MTX date of application
Item
MTX date of application
date
C0025677 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Cytarabin
Item
Cytarabin
integer
C0010711 (UMLS CUI [1])
Cytarabin date
Item
Cytarabin date
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
G-CSF
C0796404 (UMLS CUI-1)
G-CSF?
Item
G-CSF?
boolean
C0079459 (UMLS CUI [1])
PEG-Filgrastim date
Item
PEG-Filgrastim date
date
C0210630 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Filgrastim dosage
Item
Filgrastim dosage
integer
C0210630 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Filgrastim Duration of treatment
Item
Filgrastim Duration of treatment
integer
C0210630 (UMLS CUI [1,1])
C0444921 (UMLS CUI [1,2])
Item Group
Cycle duration
Interval
Item
Interval
integer
C1272706 (UMLS CUI [1])
Reason for prolonged interval
Item
Reason for prolonged interval
integer
C1272706 (UMLS CUI [1])
Item Group
Therapy discontinuation
Therapy discontinuation
Item
Therapy discontinuation
boolean
C0677162 (UMLS CUI [1])
Progressive Disease
Item
Progressive Disease
boolean
C1335499 (UMLS CUI [1])
Drug toxicity
Item
Drug toxicity
boolean
C0013221 (UMLS CUI [1])
Patient wish
Item
Patient wish
boolean
C0747309 (UMLS CUI [1])
Other
Item
Other
boolean
C0205394 (UMLS CUI [1])
Item Group
Stem Cell Mobilization
Stem Cell Mobilization
Item
Stem Cell Mobilization
boolean
C0524864 (UMLS CUI [1])
CD34 stem cell count procedure
Item
CD34 stem cell count procedure
integer
C1277788 (UMLS CUI [1])
Item Group
Lab results prior to chemotherapy cycle
C1302181 (UMLS CUI-1)
HB
Item
HB
float
C0518015 (UMLS CUI [1])
Leucocytes
Item
Leucocytes
float
C0023508 (UMLS CUI [1])
Granulocytes
Item
Granulocytes
float
C0857490 (UMLS CUI [1])
Thrombocytes
Item
Thrombocytes
float
C0005821 (UMLS CUI [1])
Creatinin
Item
Creatinin
float
C0201976 (UMLS CUI [1])
Bilirubin
Item
Bilirubin
float
C1278039 (UMLS CUI [1])
C-reactives Proteine
Item
C-reactives Proteine
float
C0006560 (UMLS CUI [1])
Other
Item
Other
float
Item Group
Lab results during interval after chemotherapy cycle
Chemotherapy cycle
Item
Chemotherapy cycle
text
C1302181 (UMLS CUI [1,1])
C3468389 (UMLS CUI [1,2])
HB
Item
HB
float
C0518015 (UMLS CUI [1])
Leucocytes
Item
Leucocytes
float
C0023508 (UMLS CUI [1])
Granulocyte count
Item
Granulocyte count
float
C0857490 (UMLS CUI [1])
Thrombozctes
Item
Thrombozctes
float
C1287267 (UMLS CUI [1])
Item Group
Toxicity
C0013221 (UMLS CUI-1)
Creatinin
Item
Creatinin
integer
C0201976 (UMLS CUI [1])
Nausea
Item
Nausea
float
C0027497 (UMLS CUI [1])
Vomiting
Item
Vomiting
integer
C0042963 (UMLS CUI [1])
Diarrhoe
Item
Diarrhoe
integer
C0011991 (UMLS CUI [1])
Stomatitis
Item
Stomatitis
integer
C0038362 (UMLS CUI [1])
Obstipation
Item
Obstipation
integer
C1963087 (UMLS CUI [1])
Stomatitis
Item
Stomatitis
integer
C0038362 (UMLS CUI [1])
Hemorrhagic cystitis
Item
Hemorrhagic cystitis
integer
C0085692 (UMLS CUI [1])
Level of consciousness
Item
Level of consciousness
integer
C0234425 (UMLS CUI [1])
Alopezie
Item
Alopezie
integer
C1559115 (UMLS CUI [1])
Infection
Item
Infection
integer
C0009450 (UMLS CUI [1])
Toxicity
Item
Toxicity
integer
C0013221 (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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