ID
25845
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.
Mots-clés
Versions (1)
- 21/09/2017 21/09/2017 -
Détendeur de droits
Glaxo Smith Kline
Téléchargé le
21 septembre 2017
DOI
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Licence
Creative Commons BY-NC 3.0
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GSK AVA100193 Rosiglitazone in Alzheimer´s Disease -Early withdrawal
Early Withdrawal and Early Withdrawal Follow-up
- StudyEvent: ODM
Description
Early Withdrawal Follow-up
Alias
- UMLS CUI-1
- C2349954
- UMLS CUI-2
- C0011008
- UMLS CUI-3
- C1710477
- UMLS CUI-4
- C3274571
Description
Investigator Instructions
Type de données
text
Alias
- UMLS CUI [1]
- C1442085
Description
Subject Identifier
Type de données
integer
Alias
- UMLS CUI [1]
- C2348585
Description
Visit Date
Type de données
date
Alias
- UMLS CUI [1]
- C1320303
Description
Weight
Type de données
float
Alias
- UMLS CUI [1]
- C0005910
Description
Blood pressure and heart rate will be measured once, after the subject sits quietly for at least 5 minutes.
Type de données
integer
Unités de mesure
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Description
Blood pressure and heart rate will be measured once, after the subject sits quietly for at least 5 minutes.
Type de données
integer
Unités de mesure
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Description
Blood pressure and heart rate will be measured once, after the subject sits quietly for at least 5 minutes.
Type de données
integer
Unités de mesure
- bpm
Alias
- UMLS CUI [1]
- C0018810
Description
Central Laboratory (Non fasting samples)
Type de données
text
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C2585491
Description
Collection Date
Type de données
date
Alias
- UMLS CUI [1]
- C1317250
Description
Concomitant Medications
Type de données
text
Alias
- UMLS CUI [1]
- C2347852
Description
Adverse Events
Type de données
text
Alias
- UMLS CUI [1]
- C0877248
Description
Note: If any abnormalities are found as a result of the physical examination, these must be recorded on the NonSerious Adverse Events page.
Type de données
text
Alias
- UMLS CUI [1]
- C0031809
Description
Press firmly with thumb anterior to the worst affected ankle until further pressure produces no greater indentation. Visually estimate depth of pit and record the Estimated Depth of Indentation below. Note: Use the same ankle throughout the study
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0574002
- UMLS CUI [1,2]
- C0205125
Description
Pedal edema
Type de données
integer
Alias
- UMLS CUI [1]
- C0574002
Description
End of Study Assessments
Type de données
text
Alias
- UMLS CUI [1,1]
- C0444496
- UMLS CUI [1,2]
- C1516048
Similar models
Early Withdrawal and Early Withdrawal Follow-up
- StudyEvent: ODM
C0011008 (UMLS CUI-2)
C1710477 (UMLS CUI-3)
C2585491 (UMLS CUI [1,2])
C0205125 (UMLS CUI [1,2])
C0011008 (UMLS CUI-2)
C1710477 (UMLS CUI-3)
C3274571 (UMLS CUI-4)
C2585491 (UMLS CUI [1,2])
C0205125 (UMLS CUI [1,2])
C1516048 (UMLS CUI [1,2])