ID

25886

Description

A 24 week double-blind, randomised, placebo-controlled, parallel-group dose-ranging study to investigate the effects of rosiglitazone (extended release tablets) on cognition in subjects with mild to moderate Alzheimer's disease.

Keywords

  1. 9/25/17 9/25/17 -
Copyright Holder

Glaxo Smith Kline

Uploaded on

September 25, 2017

DOI

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License

Creative Commons BY-NC 3.0

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GSK AVA100193 Rosiglitazone in Alzheimer´s Disease - Pharmacogenetic and Pharmacogenomic Research

Pharmacogenetic and Pharmacogenomic Research

PGx-Pharmacogenetic/PGm-Transcriptomic/PGM-Proteomic Research
Description

PGx-Pharmacogenetic/PGm-Transcriptomic/PGM-Proteomic Research

Alias
UMLS CUI-1
C2347501
UMLS CUI-2
C1327760
Has informed consent been obtained for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic Research?
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
If Yes, record the date informed consent obtained for PGxPharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research
Description

Date informed consent obtained

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0021430
If No, check
Description

reason informed consent not obtained

Data type

integer

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C1882120
If other reason please specify
Description

reason informed consent not obtained

Data type

text

Alias
UMLS CUI [1,1]
C3845569
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C1882120
Has a blood sample been collected for PGx-pharmacogenetic research?
Description

Blood sample collection

Data type

boolean

Alias
UMLS CUI [1]
C0005834
If Yes, record the date sample taken
Description

Blood sample collection date

Data type

date

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0011008
Has subject withdrawn consent for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research?
Description

Withdrawal of Consent

Data type

boolean

Alias
UMLS CUI [1,1]
C1707492
UMLS CUI [1,2]
C2347501
UMLS CUI [1,3]
C1327760
Has a request been made for sample destruction?
Description

Blood sample destruction

Data type

boolean

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

Blood sample destruction reason

Data type

text

Alias
UMLS CUI [1,1]
C1948029
UMLS CUI [1,2]
C0178913
UMLS CUI [1,3]
C0392360
Other reason for sample destruction
Description

Other reason for sample destruction

Data type

text

Alias
UMLS CUI [1,1]
C1948029
UMLS CUI [1,2]
C0178913
UMLS CUI [1,3]
C3845569

Similar models

Pharmacogenetic and Pharmacogenomic Research

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
PGx-Pharmacogenetic/PGm-Transcriptomic/PGM-Proteomic Research
C2347501 (UMLS CUI-1)
C1327760 (UMLS CUI-2)
Informed Consent
Item
Has informed consent been obtained for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic Research?
boolean
C0021430 (UMLS CUI [1])
Date informed consent obtained
Item
If Yes, record the date informed consent obtained for PGxPharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research
date
C0011008 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Item
If No, check
integer
C0392360 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C1882120 (UMLS CUI [1,3])
CL Item
Subject declined (1)
CL Item
Subject not asked by Investigator (2)
CL Item
Other (3)
reason informed consent not obtained
Item
If other reason please specify
text
C3845569 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C1882120 (UMLS CUI [1,3])
Blood sample collection
Item
Has a blood sample been collected for PGx-pharmacogenetic research?
boolean
C0005834 (UMLS CUI [1])
Blood sample collection date
Item
If Yes, record the date sample taken
date
C0005834 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Withdrawal of Consent
Item
Has subject withdrawn consent for PGx-Pharmacogenetic/PGm-Transcriptomic/PGm-Proteomic research?
boolean
C1707492 (UMLS CUI [1,1])
C2347501 (UMLS CUI [1,2])
C1327760 (UMLS CUI [1,3])
Blood sample destruction
Item
Has a request been made for sample destruction?
boolean
C1948029 (UMLS CUI [1,1])
C0178913 (UMLS CUI [1,2])
Item
If Yes, check one reason
text
C1948029 (UMLS CUI [1,1])
C0178913 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
Code List
If Yes, check one reason
CL Item
Subject requested (1)
CL Item
Other (Z)
Other reason for sample destruction
Item
Other reason for sample destruction
text
C1948029 (UMLS CUI [1,1])
C0178913 (UMLS CUI [1,2])
C3845569 (UMLS CUI [1,3])

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