ID

20058

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

Versions (2)
  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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Throughout: Hospitalization Records [HO_1] NCT01117584

Anglais

Throughout: Hospitalization Records [HO_1] NCT01117584

1 Formulaires  
General Information
Description

General Information

Was the subject hospitalized from the time of First Dose of Randomized Study Drug through Visit 9?
Description

Any Hospitalization

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0347984
UMLS CUI [1,3]
C0008972
Date of Admission
Description

Date of Admission

Type de données

date

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C1302393
Ongoing?
Description

Ongoing

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0549178
Date of Discharge
Description

Date of Discharge

Type de données

date

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C2361123
Type of Hospitalization
Description

Type of Hospitalization

Type de données

integer

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0332307
UMLS CUI [1,3]
C0021708
Reason for Hospitalization
Description

Reason for Hospitalization

Type de données

text

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0392360
If Other, please specify
Description

Other

Type de données

text

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0392360
Retour au début de la page

Similar models

Throughout: Hospitalization Records [HO_1] NCT01117584

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
General Information
Any Hospitalization
Item
Was the subject hospitalized from the time of First Dose of Randomized Study Drug through Visit 9?
boolean
C0019993 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,3])
Date of Admission
Item
Date of Admission
date
C0019993 (UMLS CUI [1,1])
C1302393 (UMLS CUI [1,2])
Ongoing
Item
Ongoing?
boolean
C0019993 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
Date of Discharge
Item
Date of Discharge
date
C0019993 (UMLS CUI [1,1])
C2361123 (UMLS CUI [1,2])
Item
Type of Hospitalization
integer
C0019993 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C0021708 (UMLS CUI [1,3])
Type of Hospitalization
Code List
Type of Hospitalization
CL Item
Non ICU (1)
CL Item
ICU (2)
Item
Reason for Hospitalization
text
C0019993 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Reason for Hospitalization
Code List
Reason for Hospitalization
CL Item
Adverse Event  (1)
CL Item
Other (2)
Other
Item
If Other, please specify
text
C0019993 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Retour au début de la page 

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