ID

14437

Beskrivning

NINDS Common Data Elements [Magnetic Resonance Imaging][Amyotrophic Lateral Sclerosis] Used from the National Institute of Neurological Disorders and Stroke Common Data Elements (https://www.commondataelements.ninds.nih.gov/) References: Grinnon ST, Miller K, Marler JR, Lu Y, Stout A, Odenkirchen J, Kunitz S. National Institute of Neurological Disorders and Stroke Common Data Element Project - approach and methods. Clin Trials. 2012;9(3):322-9.

Länk

https://www.commondataelements.ninds.nih.gov/

Nyckelord

Versioner (1)
  1. 2016-04-15 2016-04-15 -
Uppladdad den

15 april 2016

DOI

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Creative Commons BY-NC 3.0
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NINDS CDE Prior and Concomitant Medications Amyotrophic Lateral Sclerosis

Engelsk

Prior and Concomitant Medications

1 Formulär  
Prior and Concomitant Medications
Beskrivning

Prior and Concomitant Medications

Study-ID
Beskrivning

Study ID

Datatyp

integer

Alias
UMLS CUI [1]
C2826693
Study site name
Beskrivning

Study site

Datatyp

text

Alias
UMLS CUI [1]
C2825164
Subject ID
Beskrivning

Subject ID

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Did the participant/subject take any medications before or during the study?
Beskrivning

If no, leave the rest of form blank

Datatyp

boolean

Alias
UMLS CUI [1]
C2347852
Medication name
Beskrivning

(Trade or generic name)

Datatyp

text

Alias
UMLS CUI [1]
C2360065
Indication
Beskrivning

(If given for AE, enter exact term from AE CRF)

Datatyp

text

Alias
UMLS CUI [1]
C2826696
Dose
Beskrivning

Medication Dose

Datatyp

float

Alias
UMLS CUI [1]
C3174092
Units
Beskrivning

(mg, microgr,...)

Datatyp

text

Alias
UMLS CUI [1]
C1519795
Medication frequency
Beskrivning

Medication frequency

Datatyp

text

Alias
UMLS CUI [1]
C3476109
Route of administration
Beskrivning

Route of administration

Datatyp

integer

Alias
UMLS CUI [1]
C0013153
If other route of administration, please specify
Beskrivning

Route of administration

Datatyp

text

Alias
UMLS CUI [1]
C0013153
Agent Start Date (yyyy-mm-dd)
Beskrivning

Medication Start Date

Datatyp

date

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0808070
Agent End Date (yyyy-mm-dd)
Beskrivning

Medication End Date

Datatyp

date

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0808070
Medication ongoing
Beskrivning

Medication ongoing

Datatyp

boolean

Alias
UMLS CUI [1]
C2826666
Tillbaka till toppen

Similar models

Prior and Concomitant Medications

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Prior and Concomitant Medications
Study ID
Item
Study-ID
integer
C2826693 (UMLS CUI [1])
Study site
Item
Study site name
text
C2825164 (UMLS CUI [1])
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Concomitant medication
Item
Did the participant/subject take any medications before or during the study?
boolean
C2347852 (UMLS CUI [1])
Medication name
Item
Medication name
text
C2360065 (UMLS CUI [1])
Indication
Item
Indication
text
C2826696 (UMLS CUI [1])
Medication Dose
Item
Dose
float
C3174092 (UMLS CUI [1])
Units
Item
Units
text
C1519795 (UMLS CUI [1])
Medication frequency
Item
Medication frequency
text
C3476109 (UMLS CUI [1])
Item
Route of administration
integer
C0013153 (UMLS CUI [1])
Route of administration
Code List
Route of administration
CL Item
Buccal (1)
CL Item
Inhaled (2)
CL Item
Intramuscular (3)
CL Item
Intravenous (4)
CL Item
Nasal (5)
CL Item
Oral (6)
CL Item
Rectal (7)
CL Item
By ear (8)
CL Item
Topical (9)
CL Item
Subcutaneous (10)
CL Item
Sublingual (11)
CL Item
Transdermal (12)
CL Item
Unknown (13)
CL Item
Other specify (14)
Route of administration
Item
If other route of administration, please specify
text
C0013153 (UMLS CUI [1])
Medication Start Date
Item
Agent Start Date (yyyy-mm-dd)
date
C2347852 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Medication End Date
Item
Agent End Date (yyyy-mm-dd)
date
C2347852 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Medication ongoing
Item
Medication ongoing
boolean
C2826666 (UMLS CUI [1])
Tillbaka till toppen 

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