ID

19948

Description

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 Medicine: rosiglitazone, Condition: Alzheimer's Disease, Phase: 2, Clinical Study ID: AVA100468, Sponsor: GSK

Mots-clés

  1. 31/01/2017 31/01/2017 -
  2. 06/02/2017 06/02/2017 -
Téléchargé le

31 janvier 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Study Conclusion GSK-AVA100468 NCT00381238

Study Conclusion GSK-AVA100468 NCT00381238

Study Conclusion
Description

Study Conclusion

Alias
UMLS CUI-1
C1707478
Did the subject become pregnant during the study? (Check that responses provided correspond with the sex of the subject) If `Yes`, complete Pregnancy Notification
Description

Pregnancy Information

Type de données

integer

Alias
UMLS CUI [1]
C0032961
Date of subject completion or withdrawal
Description

End Date

Type de données

date

Alias
UMLS CUI [1]
C0806020
Was the subject withdrawn from the study?
Description

Withdrawal

Type de données

boolean

Alias
UMLS CUI [1]
C2349954
What was the primary reason for withdrawal?
Description

Withdrawal reason

Type de données

integer

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C1549995
What was the primary reason for withdrawal? If other, specify:
Description

Withdrawal Other

Type de données

text

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C1549995

Similar models

Study Conclusion GSK-AVA100468 NCT00381238

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Study Conclusion
C1707478 (UMLS CUI-1)
Item
Did the subject become pregnant during the study? (Check that responses provided correspond with the sex of the subject) If `Yes`, complete Pregnancy Notification
integer
C0032961 (UMLS CUI [1])
Code List
Did the subject become pregnant during the study? (Check that responses provided correspond with the sex of the subject) If `Yes`, complete Pregnancy Notification
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Applicable (not of childbearing potential or male) (3)
End Date
Item
Date of subject completion or withdrawal
date
C0806020 (UMLS CUI [1])
Withdrawal
Item
Was the subject withdrawn from the study?
boolean
C2349954 (UMLS CUI [1])
Item
What was the primary reason for withdrawal?
integer
C2349954 (UMLS CUI [1,1])
C1549995 (UMLS CUI [1,2])
Code List
What was the primary reason for withdrawal?
CL Item
Adverse event (record details on the Non-Serious Adverse Event or Serious Adverse Event pages as appropriate) (1)
CL Item
Lost to follow-up (2)
CL Item
Protocol violation (3)
CL Item
Subject decided to withdraw from the study (4)
CL Item
Sponsor terminated study (5)
CL Item
Non-compliance (6)
CL Item
Other (7)
Withdrawal Other
Item
What was the primary reason for withdrawal? If other, specify:
text
C2349954 (UMLS CUI [1,1])
C1549995 (UMLS CUI [1,2])

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