ID

29816

Beschrijving

Eze/Simva Switch Study in Diabetics (0653A-807); ODM derived from: https://clinicaltrials.gov/show/NCT00541697

Link

https://clinicaltrials.gov/show/NCT00541697

Trefwoorden

  1. 21-04-18 21-04-18 - Julian Varghese
Houder van rechten

See clinicaltrials.gov

Geüploaded op

21 april 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 2 NCT00541697

Eligibility Diabetes Mellitus, Type 2 NCT00541697

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
currently being treated with atorvastatin 10 mg for at least 6 weeks
Beschrijving

atorvastatin Unit dose

Datatype

boolean

Alias
UMLS CUI [1,1]
C0286651
UMLS CUI [1,2]
C0869039
have type 2 diabetes
Beschrijving

Diabetes Mellitus, Non-Insulin-Dependent

Datatype

boolean

Alias
UMLS CUI [1]
C0011860
weight must be stable for more than 6 weeks before entering the study
Beschrijving

Body Weight Stable Duration

Datatype

boolean

Alias
UMLS CUI [1,1]
C0005910
UMLS CUI [1,2]
C0205360
UMLS CUI [1,3]
C0449238
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
consume more than 14 alcoholic drinks per week.
Beschrijving

Alcohol consumption Drinks Weekly

Datatype

boolean

Alias
UMLS CUI [1,1]
C0001948
UMLS CUI [1,2]
C0001967
UMLS CUI [1,3]
C0332174
pregnant or lactating
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
have taken another investigation drug within 3 months of starting this study
Beschrijving

Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1]
C0013230
history of congestive heart failure, heart attack, coronary artery bypass surgery
Beschrijving

Congestive heart failure | Myocardial Infarction | Coronary Artery Bypass Surgery

Datatype

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0027051
UMLS CUI [3]
C0010055
uncontrolled high blood pressure
Beschrijving

Uncontrolled hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C1868885
hiv positive
Beschrijving

HIV Seropositivity

Datatype

boolean

Alias
UMLS CUI [1]
C0019699
history of cancer in the last 5 years
Beschrijving

Malignant Neoplasm disease length

Datatype

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0872146

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00541697

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
atorvastatin Unit dose
Item
currently being treated with atorvastatin 10 mg for at least 6 weeks
boolean
C0286651 (UMLS CUI [1,1])
C0869039 (UMLS CUI [1,2])
Diabetes Mellitus, Non-Insulin-Dependent
Item
have type 2 diabetes
boolean
C0011860 (UMLS CUI [1])
Body Weight Stable Duration
Item
weight must be stable for more than 6 weeks before entering the study
boolean
C0005910 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Alcohol consumption Drinks Weekly
Item
consume more than 14 alcoholic drinks per week.
boolean
C0001948 (UMLS CUI [1,1])
C0001967 (UMLS CUI [1,2])
C0332174 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Investigational New Drugs
Item
have taken another investigation drug within 3 months of starting this study
boolean
C0013230 (UMLS CUI [1])
Congestive heart failure | Myocardial Infarction | Coronary Artery Bypass Surgery
Item
history of congestive heart failure, heart attack, coronary artery bypass surgery
boolean
C0018802 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0010055 (UMLS CUI [3])
Uncontrolled hypertension
Item
uncontrolled high blood pressure
boolean
C1868885 (UMLS CUI [1])
HIV Seropositivity
Item
hiv positive
boolean
C0019699 (UMLS CUI [1])
Malignant Neoplasm disease length
Item
history of cancer in the last 5 years
boolean
C0006826 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])

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