Informatie:
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ID
22958
Beschrijving
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
Trefwoorden
Versies (1)
- 18-06-17 18-06-17 -
Geüploaded op
18 juni 2017
DOI
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Creative Commons BY 4.0
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Eligibility Type 2 Diabetes Mellitus NCT00437164
Eligibility Type 2 Diabetes Mellitus NCT00437164
- StudyEvent: Eligibility
Similar models
Eligibility Type 2 Diabetes Mellitus NCT00437164
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
C0006826 (UMLS CUI [2])