ID

24140

Beschrijving

Study ID: 100468 Clinical Study ID: AVA100468 Study Title: 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 Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 2 Study Recruitment Status: Completed Generic Name: rosiglitazone Trade Name: Avandia XR,Avandia; Avandia XR,Rosiglitazone XR,Avandia Study Indication: Alzheimer's Disease Concomitant Medications

Trefwoorden

Versies (1)
  1. 25-07-17 25-07-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

25 juli 2017

DOI

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Licentie

Creative Commons BY-NC-ND 3.0
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Concomitant Medications GSK Rosiglitazone Alzheimer's disease 100468

Engels

Concomitant Medications GSK Rosiglitazone Alzheimer's disease 100468

1 Formulieren  
Patient Information
Beschrijving

Patient Information

Alias
UMLS CUI-1
C1955348
Subject Identifier
Beschrijving

Subject Identifier

Datatype

text

Alias
UMLS CUI [1]
C2348585
Concomitant Medications
Beschrijving

Concomitant Medications

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

If YES, record each medication on a seperate line using Trade Names where possible. If the medication is realted to an Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.

Datatype

boolean

Drug Name (Trade name preferred) e.g. Aspirin
Beschrijving

Drug Name

Datatype

text

Alias
UMLS CUI [1]
C0013227
Total Daily Dose e.g. 400
Beschrijving

Total Daily Dose

Datatype

float

Alias
UMLS CUI [1]
C2348070
Unit (for Units and Route see facing page for examples of acceptable abbreviations) e.g. mg
Beschrijving

Unit

Datatype

text

Alias
UMLS CUI [1]
C1519795
Route (For Units and Route see facing page for examples of acceptable abbreviations) e.g. PO
Beschrijving

Administration Route

Datatype

text

Reason for Medication e.g. Headache
Beschrijving

Reason for Medication

Datatype

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013227
Start Date e.g. 31 MAY 02
Beschrijving

Start Date

Datatype

date

Maateenheden
  • dd-mmm-yy
dd-mmm-yy
Stop Date e.g. 31 MAY 02
Beschrijving

Stop Date

Datatype

date

Maateenheden
  • dd-mmm-yy
dd-mmm-yy
Ongoing Medication? e.g. N
Beschrijving

Ongoing

Datatype

text

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Similar models

Concomitant Medications GSK Rosiglitazone Alzheimer's disease 100468

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Patient Information
C1955348 (UMLS CUI-1)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Item Group
Concomitant Medications
C2347852 (UMLS CUI-1)
Concomitant Medications
Item
Were any concomitant medications taken by the subject during the study?
boolean
Drug Name
Item
Drug Name (Trade name preferred) e.g. Aspirin
text
C0013227 (UMLS CUI [1])
Total Daily Dose
Item
Total Daily Dose e.g. 400
float
C2348070 (UMLS CUI [1])
Unit
Item
Unit (for Units and Route see facing page for examples of acceptable abbreviations) e.g. mg
text
C1519795 (UMLS CUI [1])
Administration Route
Item
Route (For Units and Route see facing page for examples of acceptable abbreviations) e.g. PO
text
Reason for Medication
Item
Reason for Medication e.g. Headache
text
C0392360 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Start Date
Item
Start Date e.g. 31 MAY 02
date
Stop Date
Item
Stop Date e.g. 31 MAY 02
date
Item
Ongoing Medication? e.g. N
text
Ongoing
Code List
Ongoing Medication? e.g. N
CL Item
Yes (Y)
CL Item
No (N)
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