ID

22958

Beschreibung

A Study To Assess GW677954 Used In Combination With Insulin In Subjects Who Have Type 2 Diabetes Mellitus; ODM derived from: https://clinicaltrials.gov/show/NCT00437164

Link

https://clinicaltrials.gov/show/NCT00437164

Stichworte

  1. 18.06.17 18.06.17 -
Hochgeladen am

18. Juni 2017

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes Mellitus NCT00437164

Eligibility Type 2 Diabetes Mellitus NCT00437164

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
have been diagnosed by a doctor with type 2 diabetes mellitus at least 3 months before screening
Beschreibung

Diabetes Mellitus Type 2

Datentyp

boolean

Alias
UMLS CUI [1]
C0011860
have a body mass index within range 25 to 40.0kg/m2 inclusive
Beschreibung

BMI

Datentyp

boolean

Alias
UMLS CUI [1]
C1305855
females who meet above criteria must be physiologically incapable of becoming pregnant (ie., surgically sterilized, or post-menopausal per protocol definition)
Beschreibung

Childbearing Potential

Datentyp

boolean

Alias
UMLS CUI [1]
C3831118
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
significant weight loss or gain in the 3 months before screening
Beschreibung

Weight Loss

Datentyp

boolean

Alias
UMLS CUI [1]
C1262477
have used insulin to treat hyperglycemia within 3 months before screening
Beschreibung

Insulin Treatment

Datentyp

boolean

Alias
UMLS CUI [1]
C0745343
have a history of fluid retention
Beschreibung

Fluid Retention

Datentyp

boolean

Alias
UMLS CUI [1]
C0268000
have uncontrolled high blood pressure
Beschreibung

Uncontrolled hypertension

Datentyp

boolean

Alias
UMLS CUI [1]
C1868885
have liver disease
Beschreibung

Liver Disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0023895
take loop diuretics (water pills), certain blood thinners, and/or st. johns wort.- have or have had certain kinds of cancer
Beschreibung

Medication or cancer

Datentyp

boolean

Alias
UMLS CUI [1]
C0013227
UMLS CUI [2]
C0006826

Ähnliche Modelle

Eligibility Type 2 Diabetes Mellitus NCT00437164

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus Type 2
Item
have been diagnosed by a doctor with type 2 diabetes mellitus at least 3 months before screening
boolean
C0011860 (UMLS CUI [1])
BMI
Item
have a body mass index within range 25 to 40.0kg/m2 inclusive
boolean
C1305855 (UMLS CUI [1])
Childbearing Potential
Item
females who meet above criteria must be physiologically incapable of becoming pregnant (ie., surgically sterilized, or post-menopausal per protocol definition)
boolean
C3831118 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Weight Loss
Item
significant weight loss or gain in the 3 months before screening
boolean
C1262477 (UMLS CUI [1])
Insulin Treatment
Item
have used insulin to treat hyperglycemia within 3 months before screening
boolean
C0745343 (UMLS CUI [1])
Fluid Retention
Item
have a history of fluid retention
boolean
C0268000 (UMLS CUI [1])
Uncontrolled hypertension
Item
have uncontrolled high blood pressure
boolean
C1868885 (UMLS CUI [1])
Liver Disease
Item
have liver disease
boolean
C0023895 (UMLS CUI [1])
Medication or cancer
Item
take loop diuretics (water pills), certain blood thinners, and/or st. johns wort.- have or have had certain kinds of cancer
boolean
C0013227 (UMLS CUI [1])
C0006826 (UMLS CUI [2])

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