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

Lien

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

Mots-clés

Versions (1)
  1. 29/05/2017 29/05/2017 -
Téléchargé le

29 mai 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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

Anglais

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

1 Formulaires  
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

Type de données

boolean

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

Date

Type de données

date

Unités de mesure
  • 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

Type de données

integer

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

Specification

Type de données

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

Type de données

boolean

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

Date sample taken

Type de données

date

Unités de mesure
  • 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Has this subject withdrawn consent for Pharmacogenetic Research?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

Type de données

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

Type de données

boolean

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

Reason for Sample Destruction

Type de données

integer

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

Specification

Type de données

text

Alias
UMLS CUI [1,1]
C0178913
UMLS CUI [1,2]
C1948029
UMLS CUI [1,3]
C2348235
Retour au début de la page

Similar models

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

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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