ID

20047

Beskrivning

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.

Nyckelord

  1. 2016-12-29 2016-12-29 -
  2. 2017-02-04 2017-02-04 -
Uppladdad den

4 februari 2017

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :


Inga kommentarer

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Dosing Study Drug: Oral [EX 6] NCT01117584

Dosing Study Drug: Oral [EX 6] NCT01117584

General Information
Beskrivning

General Information

Type of Study Drug
Beskrivning

Type of Study Drug

Datatyp

integer

Alias
UMLS CUI [1]
C0457591
Not done
Beskrivning

Not done

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C1272696
Date of first dose
Beskrivning

Date of first dose

Datatyp

date

Alias
UMLS CUI [1]
C3173309
Study day of start of treatment
Beskrivning

Study day of start of treatment

Datatyp

text

Alias
UMLS CUI [1,1]
C3173309
UMLS CUI [1,2]
C2826182
Date of last dose
Beskrivning

Date of last dose

Datatyp

date

Alias
UMLS CUI [1]
C1762893
Study day of end of treatment
Beskrivning

Study day of end of treatment

Datatyp

text

Alias
UMLS CUI [1,1]
C1762893
UMLS CUI [1,2]
C2826182

Similar models

Dosing Study Drug: Oral [EX 6] NCT01117584

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
General Information
Item
Type of Study Drug
integer
C0457591 (UMLS CUI [1])
Code List
Type of Study Drug
CL Item
Run-In Medication (1)
CL Item
Randomized Study Drug (2)
Not done
Item
Not done
boolean
C0013216 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Date of first dose
Item
Date of first dose
date
C3173309 (UMLS CUI [1])
Study day of start of treatment
Item
Study day of start of treatment
text
C3173309 (UMLS CUI [1,1])
C2826182 (UMLS CUI [1,2])
Date of last dose
Item
Date of last dose
date
C1762893 (UMLS CUI [1])
Study day of end of treatment
Item
Study day of end of treatment
text
C1762893 (UMLS CUI [1,1])
C2826182 (UMLS CUI [1,2])

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial