ID

34585

Description

A Study to Assess the Pharmacokinetics, Pharmacodynamics of ASP1941 in Diabetes Mellitus Patients With Renal Impairment; ODM derived from: https://clinicaltrials.gov/show/NCT01097681

Link

https://clinicaltrials.gov/show/NCT01097681

Keywords

  1. 1/19/19 1/19/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 19, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes Mellitus NCT01097681

Eligibility Type 2 Diabetes Mellitus NCT01097681

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetic patients for at least 12 weeks
Description

ID.1

Data type

boolean

fasting plasma glucose level of < 240 mg/dl
Description

ID.2

Data type

boolean

body mass index ( bmi )20.0 - 35.0kg/m2
Description

ID.3

Data type

boolean

gfr value based on the japanese gfr estimation equation at screening, of ≥ 30 ml/min/1.73m2
Description

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
type 1 diabetes mellitus patients
Description

ID.5

Data type

boolean

receiving insulin within 12 weeks before screening
Description

ID.6

Data type

boolean

diabetic ketoacidosis
Description

ID.7

Data type

boolean

dysuria and/or urinary tract infection, genital infection
Description

ID.8

Data type

boolean

significant renal, hepatic or cardiovascular diseases
Description

ID.9

Data type

boolean

severe gastrointestinal diseases
Description

ID.10

Data type

boolean

Similar models

Eligibility Type 2 Diabetes Mellitus NCT01097681

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
type 2 diabetic patients for at least 12 weeks
boolean
ID.2
Item
fasting plasma glucose level of < 240 mg/dl
boolean
ID.3
Item
body mass index ( bmi )20.0 - 35.0kg/m2
boolean
ID.4
Item
gfr value based on the japanese gfr estimation equation at screening, of ≥ 30 ml/min/1.73m2
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
type 1 diabetes mellitus patients
boolean
ID.6
Item
receiving insulin within 12 weeks before screening
boolean
ID.7
Item
diabetic ketoacidosis
boolean
ID.8
Item
dysuria and/or urinary tract infection, genital infection
boolean
ID.9
Item
significant renal, hepatic or cardiovascular diseases
boolean
ID.10
Item
severe gastrointestinal diseases
boolean

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