Concomitant Medication AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

Concomitant Medication
Beschreibung

Concomitant Medication

Alias
UMLS CUI-1
C2347852
Point in time
Beschreibung

Point in time

Datentyp

integer

Alias
UMLS CUI [1,1]
C1276413
UMLS CUI [1,2]
C2348792
If Maintenance: Month
Beschreibung

Maintenance Month

Datentyp

integer

Maßeinheiten
  • Month
Alias
UMLS CUI [1,1]
C0481504
UMLS CUI [1,2]
C0439231
Pharmalogical Substance
Beschreibung

Pharmalogical Substance

Datentyp

text

Alias
UMLS CUI [1]
C0013227
Dose
Beschreibung

Dose

Datentyp

integer

Alias
UMLS CUI [1]
C0178602
Unit
Beschreibung

Unit

Datentyp

text

Alias
UMLS CUI-1
C0869039
Application
Beschreibung

Application

Datentyp

text

Alias
UMLS CUI [1]
C0185125
Frequency
Beschreibung

Frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
Medical indication
Beschreibung

Medical indication

Datentyp

text

Alias
UMLS CUI-1
C2315323
Start Date of Medication
Beschreibung

Start Date of Medication

Datentyp

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0808070
Stop Date Medication
Beschreibung

Stop Date

Datentyp

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0806020
Signature
Beschreibung

Signature

Date
Beschreibung

Date

Datentyp

date

Alias
UMLS CUI-1
C0011008
Name of Investigator
Beschreibung

Name of Investigator

Datentyp

text

Alias
UMLS CUI-1
C2826892
Signature of investigator
Beschreibung

Signature of investigator

Datentyp

text

Alias
UMLS CUI-1
C2346576

Ähnliche Modelle

Concomitant Medication AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
Item
Point in time
integer
C1276413 (UMLS CUI [1,1])
C2348792 (UMLS CUI [1,2])
Code List
Point in time
CL Item
Diagnostic (0)
C0086143 (UMLS CUI-1)
CL Item
Induction I (1)
C3179010 (UMLS CUI-1)
CL Item
Induction II (optional) (2)
C3179010 (UMLS CUI-1)
CL Item
Consolid. I (3)
C3179017 (UMLS CUI-1)
CL Item
Consolid. II (4)
C3179017 (UMLS CUI-1)
CL Item
Consolid. III (5)
C3179017 (UMLS CUI-1)
CL Item
Consolid. IV (6)
C3179017 (UMLS CUI-1)
CL Item
Maintenance (7)
C0481504 (UMLS CUI-1)
Item
If Maintenance: Month
integer
C0481504 (UMLS CUI [1,1])
C0439231 (UMLS CUI [1,2])
Code List
If Maintenance: Month
CL Item
after 1 Month (1)
C0439231 (UMLS CUI-1)
C0205447 (UMLS CUI-2)
CL Item
after 2 Month (2)
C0439231 (UMLS CUI-1)
C0205448 (UMLS CUI-2)
CL Item
after 3 Month (3)
C0439231 (UMLS CUI-1)
C0205449 (UMLS CUI-2)
CL Item
after 4 Month (4)
C0439231 (UMLS CUI-1)
C0205450 (UMLS CUI-2)
CL Item
after 5 Month (5)
C0439231 (UMLS CUI-1)
C0205451 (UMLS CUI-2)
CL Item
after 6 Month (6)
C0439231 (UMLS CUI-1)
C0205452 (UMLS CUI-2)
CL Item
after 7 Month (7)
C0439231 (UMLS CUI-1)
C0205453 (UMLS CUI-2)
CL Item
after 8 Month (8)
C0439231 (UMLS CUI-1)
C0205454 (UMLS CUI-2)
CL Item
after 9 Month (9)
C0439231 (UMLS CUI-1)
C0205455 (UMLS CUI-2)
CL Item
after 10 Month (10)
C0439231 (UMLS CUI-1)
C0205456 (UMLS CUI-2)
CL Item
after 11 Month (11)
C0439231 (UMLS CUI-1)
C0205457 (UMLS CUI-2)
CL Item
after 12 Month (12)
C0439231 (UMLS CUI-1)
C0205458 (UMLS CUI-2)
Pharmalogical Substance
Item
Pharmalogical Substance
text
C0013227 (UMLS CUI [1])
Dose
Item
Dose
integer
C0178602 (UMLS CUI [1])
Unit
Item
Unit
text
C0869039 (UMLS CUI-1)
Item
Application
text
C0185125 (UMLS CUI [1])
Code List
Application
CL Item
oral (1)
C0442027 (UMLS CUI-1)
CL Item
intravenous (2)
C0348016 (UMLS CUI-1)
CL Item
intramuscular (3)
C0442117 (UMLS CUI-1)
CL Item
subcutaneous (4)
C0443315 (UMLS CUI-1)
CL Item
sublingual (5)
C0001565 (UMLS CUI-1)
CL Item
rectal (6)
C0205052 (UMLS CUI-1)
CL Item
Inhalation (7)
C0205535 (UMLS CUI-1)
CL Item
topical (8)
C0332237 (UMLS CUI-1)
CL Item
other (9)
C0205394 (UMLS CUI-1)
Frequency
Item
Frequency
text
C3476109 (UMLS CUI [1])
Medical indication
Item
Medical indication
text
C2315323 (UMLS CUI-1)
Start Date of Medication
Item
Start Date of Medication
date
C0013227 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Stop Date
Item
Stop Date Medication
date
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Item Group
Signature
Date
Item
Date
date
C0011008 (UMLS CUI-1)
Name of Investigator
Item
Name of Investigator
text
C2826892 (UMLS CUI-1)
Signature of investigator
Item
Signature of investigator
text
C2346576 (UMLS CUI-1)