ID

19391

Beschrijving

Cardiovascular (CV) Risk Evaluation In Type 2 Diabetes Subjects; ODM derived from: https://clinicaltrials.gov/show/NCT00648284

Link

https://clinicaltrials.gov/show/NCT00648284

Trefwoorden

  1. 28-12-16 28-12-16 -
Geüploaded op

28 december 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes Mellitus NCT00648284

Eligibility Type 2 Diabetes Mellitus NCT00648284

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with diabetes type 2 that their physician has decided to prescribe avandia for better control of their condition
Beschrijving

Diabetes Mellitus, Non-Insulin-Dependent | Disorder control Due to Avandia

Datatype

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2,1]
C0920467
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C0875967
have signed informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with alt > 2.5x the normal value
Beschrijving

Alanine aminotransferase increased

Datatype

boolean

Alias
UMLS CUI [1]
C0151905
with heart failure symptoms
Beschrijving

Symptoms in heart failure patients

Datatype

boolean

Alias
UMLS CUI [1]
C2735647
with diagnosis of angina pectoris or stable angina demanding continuous treatment with nitrates
Beschrijving

Angina Pectoris | Stable angina Requirement Nitrates

Datatype

boolean

Alias
UMLS CUI [1]
C0002962
UMLS CUI [2,1]
C0340288
UMLS CUI [2,2]
C1514873
UMLS CUI [2,3]
C0028125
with recent myocardial infarction (<6 months)
Beschrijving

Myocardial Infarction

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
with severe renal disfunction
Beschrijving

Renal dysfunction Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C3279454
UMLS CUI [1,2]
C0205082
pregnant or lactating or planned to be pregnant during the study
Beschrijving

Pregnancy | Breast Feeding | Pregnancy, Planned

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
under investigational drug treatment
Beschrijving

Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1]
C0013230
alcoholic or drug abuser
Beschrijving

Substance Use Disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0038586

Similar models

Eligibility Type 2 Diabetes Mellitus NCT00648284

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent | Disorder control Due to Avandia
Item
patients with diabetes type 2 that their physician has decided to prescribe avandia for better control of their condition
boolean
C0011860 (UMLS CUI [1])
C0920467 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0875967 (UMLS CUI [2,3])
Informed Consent
Item
have signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Alanine aminotransferase increased
Item
patients with alt > 2.5x the normal value
boolean
C0151905 (UMLS CUI [1])
Symptoms in heart failure patients
Item
with heart failure symptoms
boolean
C2735647 (UMLS CUI [1])
Angina Pectoris | Stable angina Requirement Nitrates
Item
with diagnosis of angina pectoris or stable angina demanding continuous treatment with nitrates
boolean
C0002962 (UMLS CUI [1])
C0340288 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0028125 (UMLS CUI [2,3])
Myocardial Infarction
Item
with recent myocardial infarction (<6 months)
boolean
C0027051 (UMLS CUI [1])
Renal dysfunction Severe
Item
with severe renal disfunction
boolean
C3279454 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
pregnant or lactating or planned to be pregnant during the study
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Investigational New Drugs
Item
under investigational drug treatment
boolean
C0013230 (UMLS CUI [1])
Substance Use Disorders
Item
alcoholic or drug abuser
boolean
C0038586 (UMLS CUI [1])

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