ID

20125

Beskrivning

An open-label extension to study AVA100193, to assess the long-term safety and efficacy of rosiglitazone (extended release tablets) in subjects with mild to moderate Alzheimer's disease Medicine: rosiglitazone, Condition: Alzheimer's Disease, Phase: 2, Clinical Study ID: AVA100468, Sponsor: GSK

Nyckelord

  1. 2017-01-31 2017-01-31 -
  2. 2017-02-08 2017-02-08 -
Uppladdad den

8 februari 2017

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Running Logs Concomitant Medications GSK-AVA100468 NCT00381238

Running Logs Concomitant Medications GSK-AVA100468 NCT00381238

Concomitant medications
Beskrivning

Concomitant medications

Alias
UMLS CUI-1
C2347852
Were any concomitant medications taken by the subject during the study?
Beskrivning

Concomitant medications

Datatyp

boolean

Alias
UMLS CUI [1]
C2347852
Drug name
Beskrivning

Drug name

Datatyp

text

Alias
UMLS CUI [1]
C0013227
Total Daily Dose
Beskrivning

Total Daily Dose

Datatyp

text

Alias
UMLS CUI [1]
C2348070
Units
Beskrivning

Units

Datatyp

integer

Alias
UMLS CUI [1]
C1519795
Route
Beskrivning

Route

Datatyp

integer

Alias
UMLS CUI [1]
C0013153
Reason for Medication
Beskrivning

Reason for Medication

Datatyp

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013227
Start Date
Beskrivning

Start Date

Datatyp

date

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

Stop Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0013227
Ongoing Medication?
Beskrivning

Ongoing Medication

Datatyp

boolean

Alias
UMLS CUI [1]
C2826666

Similar models

Running Logs Concomitant Medications GSK-AVA100468 NCT00381238

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Concomitant medications
C2347852 (UMLS CUI-1)
Concomitant medications
Item
Were any concomitant medications taken by the subject during the study?
boolean
C2347852 (UMLS CUI [1])
Drug name
Item
Drug name
text
C0013227 (UMLS CUI [1])
Total Daily Dose
Item
Total Daily Dose
text
C2348070 (UMLS CUI [1])
Item
Units
integer
C1519795 (UMLS CUI [1])
Code List
Units
CL Item
Tablet (1)
CL Item
Microlitre (2)
CL Item
Millilitre (3)
CL Item
Litre (4)
CL Item
Microgram (5)
CL Item
Milligram (6)
CL Item
Gram (7)
Item
Route
integer
C0013153 (UMLS CUI [1])
Code List
Route
CL Item
Intramuscular (1)
CL Item
Inhalation (2)
CL Item
Intravenous (3)
CL Item
Nasal (4)
CL Item
Topical (5)
CL Item
Oral (6)
CL Item
Vaginal (7)
Reason for Medication
Item
Reason for Medication
text
C0392360 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Ongoing Medication
Item
Ongoing Medication?
boolean
C2826666 (UMLS CUI [1])

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial