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

Concomitant Medication
Beschrijving

Concomitant Medication

Point in time
Beschrijving

Point in time

Datatype

integer

Alias
UMLS CUI-1
C1442880
If Maintenance: Month
Beschrijving

Maintenance Month

Datatype

integer

Maateenheden
  • Month
Alias
UMLS CUI-1
C0481504
UMLS CUI-2
C0439231
Agent/Tradename
Beschrijving

Agent/Tradename

Datatype

text

Alias
UMLS CUI-1
C1254351
UMLS CUI-2
C0282291
Dose
Beschrijving

Dose

Datatype

integer

Alias
UMLS CUI-1
C3174092
Unit
Beschrijving

Unit

Datatype

text

Alias
UMLS CUI-1
C0869039
Application
Beschrijving

Application

Datatype

text

Alias
UMLS CUI-1
C0185125
Frequency
Beschrijving

Frequency

Datatype

text

Alias
UMLS CUI-1
C3476109
Medical indication
Beschrijving

Medical indication

Datatype

text

Alias
UMLS CUI-1
C2315323
Start Date of Medication
Beschrijving

Start Date of Medication

Datatype

date

Alias
UMLS CUI-1
C0808070
UMLS CUI-2
C0802004
Stop Date Medication
Beschrijving

Stop Date

Datatype

date

Alias
UMLS CUI-1
C0802004
UMLS CUI-2
C0806020
Signature
Beschrijving

Signature

Date
Beschrijving

Date

Datatype

date

Alias
UMLS CUI-1
C0011008
Name of Investigator
Beschrijving

Name of Investigator

Datatype

text

Alias
UMLS CUI-1
C2826892
Signature of investigator
Beschrijving

Signature of investigator

Datatype

text

Alias
UMLS CUI-1
C2346576

Similar models

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

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Concomitant Medication
Item
Point in time
integer
C1442880 (UMLS CUI-1)
Code List
Point in time
CL Item
Diagnostic (0)
CL Item
Induction I (1)
CL Item
Induction II (optional) (2)
CL Item
Consolid. I (3)
CL Item
Consolid. II (4)
CL Item
Consolid. III (5)
CL Item
Consolid. IV (6)
CL Item
Maintenance (7)
Item
If Maintenance: Month
integer
C0481504 (UMLS CUI-1)
C0439231 (UMLS CUI-2)
Code List
If Maintenance: Month
CL Item
after 1 Month (1)
CL Item
after 2 Month (2)
CL Item
after 3 Month (3)
CL Item
after 4 Month (4)
CL Item
after 5 Month (5)
CL Item
after 6 Month (6)
CL Item
after 7 Month (7)
CL Item
after 8 Month (8)
CL Item
after 9 Month (9)
CL Item
after 10 Month (10)
CL Item
after 11 Month (11)
CL Item
after 12 Month (12)
Agent/Tradename
Item
Agent/Tradename
text
C1254351 (UMLS CUI-1)
C0282291 (UMLS CUI-2)
Dose
Item
Dose
integer
C3174092 (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)
CL Item
intravenous (2)
CL Item
intramuscular (3)
CL Item
subcutaneous (4)
CL Item
sublingual (5)
CL Item
rectal (6)
CL Item
Inhalation (7)
CL Item
topical (8)
CL Item
other (9)
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
C0808070 (UMLS CUI-1)
C0802004 (UMLS CUI-2)
Stop Date
Item
Stop Date Medication
date
C0802004 (UMLS CUI-1)
C0806020 (UMLS CUI-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)