ID

24140

Beskrivning

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

Nyckelord

Versioner (1)
  1. 2017-07-25 2017-07-25 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

25 juli 2017

DOI

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Licens

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

Engelsk

Concomitant Medications GSK Rosiglitazone Alzheimer's disease 100468

1 Formulär  
Patient Information
Beskrivning

Patient Information

Alias
UMLS CUI-1
C1955348
Subject Identifier
Beskrivning

Subject Identifier

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Concomitant Medications
Beskrivning

Concomitant Medications

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

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.

Datatyp

boolean

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

Drug Name

Datatyp

text

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

Total Daily Dose

Datatyp

float

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

Unit

Datatyp

text

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

Administration Route

Datatyp

text

Reason for Medication e.g. Headache
Beskrivning

Reason for Medication

Datatyp

text

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

Start Date

Datatyp

date

Måttenheter
  • dd-mmm-yy
dd-mmm-yy
Stop Date e.g. 31 MAY 02
Beskrivning

Stop Date

Datatyp

date

Måttenheter
  • dd-mmm-yy
dd-mmm-yy
Ongoing Medication? e.g. N
Beskrivning

Ongoing

Datatyp

text

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Similar models

Concomitant Medications GSK Rosiglitazone Alzheimer's disease 100468

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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