Informazione:
Errore:
ID
20054
Descrizione
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.
Keywords
versioni (2)
- 30/12/16 30/12/16 -
- 04/02/17 04/02/17 -
Caricato su
4 febbraio 2017
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 3.0
Commenti del modello :
Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.
Commenti del gruppo di articoli per :
Commenti dell'articolo per :
Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.
End of Study: End of Treatment/ Premature Discontinuation [DS_1] NCT01117584
End of Study: End of Treatment/ Premature Discontinuation [DS_1] NCT01117584
Similar models
End of Study: End of Treatment/ Premature Discontinuation [DS_1] NCT01117584
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Date of Collection
Item
Date of Last Treatment Evaluation Through Visit 7
datetime
C0557980 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C1517741 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Study day of collection
Item
Study day of collection
text
C0557980 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,3])
C1517741 (UMLS CUI [1,2])
C2826182 (UMLS CUI [1,3])
Complete Study Drug Treatment
Item
Did subject complete Study Drug Treatment?
boolean
C0008972 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0013216 (UMLS CUI [1,3])
C0205197 (UMLS CUI [1,4])
C0087111 (UMLS CUI [1,2])
C0013216 (UMLS CUI [1,3])
C0205197 (UMLS CUI [1,4])
Study Drug Treatment
Item
If no, please provide details below.
text
C0008972 (UMLS CUI [1,1])
C0013216 (UMLS CUI [1,2])
C1522508 (UMLS CUI [1,3])
C0013216 (UMLS CUI [1,2])
C1522508 (UMLS CUI [1,3])
CL Item
Not fulfill inclusion or exclusion criteria (1)
CL Item
Adverse event (2)
CL Item
Lack of efficacy (3)
CL Item
Withdrawal by subject (4)
CL Item
Subject lost to follow-up (5)
CL Item
Protocol violation (6)
CL Item
Randomized/registered but never received/dispensed study drug (7)
CL Item
Other (8)
Item
If reason is `Withdrawal by Subject` please speficy follow-up allowance
integer
C0589120 (UMLS CUI [1])
Code List
If reason is `Withdrawal by Subject` please speficy follow-up allowance
CL Item
Allows follow-up after withdrawal (1)
CL Item
Does not allow follow-up after withdrawal (2)
Date of Withdrawal
Item
Date of Withdrawal
date
C2349954 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Protocol Violation
Item
If "Protocol Violation", please specify
text
C1709750 (UMLS CUI [1])
Other
Item
If "Other" please specify
text