ID

20055

Description

NCT01117584 Astellas Phase 2b, Double-Blind, Randomized, Multicenter, Parallel Group, Placebo-Controlled, Dose-Finding Study to Evaluate the Efficacy, Safety and Tolerability of a 12- Week Treatment with ASP1941 in Combination with Metformin in Patients with Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control on Metformin Alone.

Mots-clés

  1. 30/12/2016 30/12/2016 -
  2. 04/02/2017 04/02/2017 -
Téléchargé le

4 février 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

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End of Study: End of Study Post-Study Period [DS_2] NCT01117584

End of Study: End of Study Post-Study Period [DS_2] NCT01117584

General Information
Description

General Information

Date of Last Evaluation
Description

Date of Last Evaluation

Type de données

date

Alias
UMLS CUI [1,1]
C0220825
UMLS CUI [1,2]
C1517741
UMLS CUI [1,3]
C0011008
Study day of collection
Description

Study day of collection

Type de données

text

Alias
UMLS CUI [1,1]
C0220825
UMLS CUI [1,2]
C1517741
UMLS CUI [1,3]
C2826182
End of Study Assessment
Description

End of Study Assessment

Type de données

integer

Alias
UMLS CUI [1,1]
C0220825
UMLS CUI [1,2]
C0008972
UMLS CUI [1,3]
C0444930
Details of Withdrawal
Description

Details of Withdrawal

Type de données

text

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C1522508
If Other, please specify
Description

Other

Type de données

text

Similar models

End of Study: End of Study Post-Study Period [DS_2] NCT01117584

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
General Information
Date of Last Evaluation
Item
Date of Last Evaluation
date
C0220825 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Study day of collection
Item
Study day of collection
text
C0220825 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,3])
Item
End of Study Assessment
integer
C0220825 (UMLS CUI [1,1])
C0008972 (UMLS CUI [1,2])
C0444930 (UMLS CUI [1,3])
Code List
End of Study Assessment
CL Item
Completed (1)
CL Item
Death (2)
CL Item
Lost to Follow-up (3)
CL Item
Withdrawal by Subject (4)
CL Item
Not Applicable (5)
CL Item
Other (6)
Details of Withdrawal
Item
Details of Withdrawal
text
C2349954 (UMLS CUI [1,1])
C1522508 (UMLS CUI [1,2])
Other
Item
If Other, please specify
text

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