ID

20058

Descripción

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.

Palabras clave

  1. 30/12/16 30/12/16 -
  2. 4/2/17 4/2/17 -
Subido en

4 de febrero de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0

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Throughout: Hospitalization Records [HO_1] NCT01117584

Throughout: Hospitalization Records [HO_1] NCT01117584

General Information
Descripción

General Information

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

Any Hospitalization

Tipo de datos

boolean

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

Date of Admission

Tipo de datos

date

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

Ongoing

Tipo de datos

boolean

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

Date of Discharge

Tipo de datos

date

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

Type of Hospitalization

Tipo de datos

integer

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

Reason for Hospitalization

Tipo de datos

text

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

Other

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0392360

Similar models

Throughout: Hospitalization Records [HO_1] NCT01117584

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])
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])
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])

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