ID

22320

Description

A Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Investigate the Effects of Rosiglitazone (Extended Release Tablets) on Cerebral Glucose Utilization and Cognition in Subjects With Mild to Moderate Alzheimer's Disease (AD) Medicine: rosiglitazone, Condition: Alzheimer's Disease, Phase: 2, Clinical Study ID: 49653/461, Sponsor: GSK Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00265148?term=NCT00265148&rank=1

Link

https://clinicaltrials.gov/ct2/show/NCT00265148?term=NCT00265148&rank=1

Keywords

Versions (1)
  1. 5/29/17 5/29/17 -
Uploaded on

May 29, 2017

DOI

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License

Creative Commons BY-NC 3.0
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Pharmacogenetic Research Effects of Rosiglitazone on Cerebral Glucose Utilization and Cognition in Subjects With Alzheimer's Disease NCT00265148

English

Pharmacogenetic Research Effects of Rosiglitazone on Cerebral Glucose Utilization and Cognition in Subjects With Alzheimer's Disease NCT00265148

1 forms  
Consent for Pharmacogenetic Research
Description

Consent for Pharmacogenetic Research

Alias
UMLS CUI-1
C2347500
Has informed consent been obtained for Pharmacogenetic Research?
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C2347500
If Yes, record the date informed consent for Pharmacogenetic Research:
Description

Date

Data type

date

Measurement units
  • dd/mm/yy
Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C2347500
UMLS CUI [1,3]
C0011008
dd/mm/yy
If no, check one reason:
Description

Reason

Data type

integer

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0392360
Specify other
Description

Specification

Data type

text

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C2348235
Blood Sample Collection
Description

Blood Sample Collection

Alias
UMLS CUI-1
C0005834
Has a blood sample been collected for Pharmacogenetic Research?
Description

Blood Sample Collection

Data type

boolean

Alias
UMLS CUI [1]
C0005834
If YES, record the date sample was taken:
Description

Date sample taken

Data type

date

Measurement units
  • dd/mm/yy
Alias
UMLS CUI [1]
C1302413
dd/mm/yy
Withdrawal of Consent
Description

Withdrawal of Consent

Alias
UMLS CUI-1
C1707492
Has this subject withdrawn consent for Pharmacogenetic Research?
Description

Withdrawal of Consent

Data type

boolean

Alias
UMLS CUI [1]
C1707492
Blood Sample Destruction
Description

Blood Sample Destruction

Alias
UMLS CUI-1
C0178913
UMLS CUI-2
C1948029
Has a request been made for sample destruction?
Description

Request for Sample Destruction

Data type

boolean

Alias
UMLS CUI [1,1]
C0178913
UMLS CUI [1,2]
C1948029
If YES, check one reason
Description

Reason for Sample Destruction

Data type

integer

Alias
UMLS CUI [1,1]
C0178913
UMLS CUI [1,2]
C1948029
UMLS CUI [1,3]
C0392360
Specify other
Description

Specification

Data type

text

Alias
UMLS CUI [1,1]
C0178913
UMLS CUI [1,2]
C1948029
UMLS CUI [1,3]
C2348235
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Similar models

Pharmacogenetic Research Effects of Rosiglitazone on Cerebral Glucose Utilization and Cognition in Subjects With Alzheimer's Disease NCT00265148

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Consent for Pharmacogenetic Research
C2347500 (UMLS CUI-1)
Informed Consent
Item
Has informed consent been obtained for Pharmacogenetic Research?
boolean
C0021430 (UMLS CUI [1,1])
C2347500 (UMLS CUI [1,2])
Date
Item
If Yes, record the date informed consent for Pharmacogenetic Research:
date
C0021430 (UMLS CUI [1,1])
C2347500 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
If no, check one reason:
integer
C0021430 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Reason
Code List
If no, check one reason:
CL Item
Subject declined (1)
CL Item
Subject not asked by Investigator (2)
CL Item
Other, specify (3)
Specification
Item
Specify other
text
C0021430 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item Group
Blood Sample Collection
C0005834 (UMLS CUI-1)
Blood Sample Collection
Item
Has a blood sample been collected for Pharmacogenetic Research?
boolean
C0005834 (UMLS CUI [1])
Date sample taken
Item
If YES, record the date sample was taken:
date
C1302413 (UMLS CUI [1])
Item Group
Withdrawal of Consent
C1707492 (UMLS CUI-1)
Withdrawal of Consent
Item
Has this subject withdrawn consent for Pharmacogenetic Research?
boolean
C1707492 (UMLS CUI [1])
Item Group
Blood Sample Destruction
C0178913 (UMLS CUI-1)
C1948029 (UMLS CUI-2)
Request for Sample Destruction
Item
Has a request been made for sample destruction?
boolean
C0178913 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
Item
If YES, check one reason
integer
C0178913 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
Reason for Sample Destruction
Code List
If YES, check one reason
CL Item
Subject requested (1)
CL Item
Screen failure (2)
CL Item
Other, specify (3)
Specification
Item
Specify other
text
C0178913 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
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