Eligibility NCT00261352 Type 2 Diabetes

ODM derived from http://clinicaltrials.gov/show/NCT00261352

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Einschlusskriterien
Age
Item
Alter 18 Jahre und älter
boolean
informed consent
Item
Provision of a written informed consent
boolean
Female patients: postmenopausal, hysterectomized, or if of childbearing potential, using a method of birth control
Item
Female patients: postmenopausal, hysterectomized, or if of childbearing potential, using a reliable method of birth control
boolean
type 2 diabetes
Item
Diagnosed with type 2 diabetes
boolean
Treatment with diet alone or with a single oral antidiabetic agent or two oral antidiabetic agents
Item
Treated with diet alone or treatment with a single oral antidiabetic agent or low doses of two oral antidiabetic agents
boolean
Item Group
Ausschlusskriterien
Type 1 diabetes
Item
Type 1 diabetes
boolean
NYHA Class III or IV
Item
New York Heart Association heart failure Class III or IV
boolean
Treatment with insulin
Item
Treatment with chronic insulin
boolean
hypersensitivity or intolerance to any peroxisome proliferator-activated receptor agonist, fenofibrate, metformin or 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor
Item
History of hypersensitivity or intolerance to any peroxisome proliferator-activated receptor agonist (like Actos or Avandia), fenofibrate, metformin or 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor (statin)
boolean
drug-induced myopathy or drug-induced creatine kinase elevation, liver enzyme elevations, neutropenia
Item
History of drug-induced myopathy or drug-induced creatine kinase elevation, liver enzyme elevations, neutropenia (low white blood cells)
boolean
Creatinine levels abnormal
Item
Creatinine levels above the normal range
boolean
Received any investigational product in other clinical studies
Item
Received any investigational product in other clinical studies within 12 weeks
boolean
Any clinically significant abnormality, which in the judgment of the investigator would compromise the patient's safety or successful participation in the clinical study
Item
Any clinically significant abnormality identified on physical examination, laboratory tests or electrocardiogram, which in the judgment of the investigator would compromise the patient's safety or successful participation in the clinical study
boolean
Item Group
Medizinische Konzepte
Age
Item
Alter
integer
C0001779 (UMLS CUI)
397669002 (SNOMED CT 2010_0731)
Diagnosis
Item
Diagnose
string
C0011900 (UMLS CUI)
439401001 (SNOMED CT 2010_0731)
MTHU008876 (LOINC Version 232)
Informed Consent
Item
Einverständniserklärung
string
C0021430 (UMLS CUI)
Postmenopause
Item
Postmenopause
string
C0206159 (UMLS CUI)
10051775 (MedDRA 13.1)
Hysterectomy
Item
Hysterektomie
string
C0020699 (UMLS CUI)
236886002 (SNOMED CT 2010_0731)
10021151 (MedDRA 13.1)
Contraception
Item
Kontrazeption
string
C0700589 (UMLS CUI)
146680009 (SNOMED CT 2010_0731)
10010808 (MedDRA 13.1)
Diabetes mellitus type 2
Item
Diabetes mellitus Typ II
string
C0011860 (UMLS CUI)
44054006 (SNOMED CT 2010_0731)
10012613 (MedDRA 13.1)
E08-E13 (ICD-10-CM Version 2010)
Diet
Item
Diät
string
C0012155 (UMLS CUI)
41829006 (SNOMED CT 2010_0731)
Anti-diabetic Agent
Item
Antidiabetikum
string
C0935929 (UMLS CUI)
373245004 (SNOMED CT 2010_0731)
Diabetes mellitus type 1
Item
Diabetes Mellitus, Insulin-Dependent
string
C0011854 (UMLS CUI)
46635009 (SNOMED CT 2010_0731)
10067584 (MedDRA 13.1)
MTHU020217 (LOINC Version 232)
E10 (ICD-10-CM Version 2010)
Heart failure
Item
Heart failure
string
C0018801 (UMLS CUI)
155374007 (SNOMED CT 2010_0731)
10019279 (MedDRA 13.1)
428 (ICD-9-CM Version 2011)
E10124 (CTCAE Version 4.03)
NYHA Class III
Item
New York Heart Association Class III
string
C1319795 (UMLS CUI)
420913000 (SNOMED CT 2010_0731)
10064081 (MedDRA 13.1)
NYHA Class IV
Item
New York Heart Association Class IV
string
C1319796 (UMLS CUI)
422293003 (SNOMED CT 2010_0731)
10064082 (MedDRA 13.1)
Therapeutic Insulin
Item
Therapeutic Insulin
string
C0557978 (UMLS CUI)
Insulin
Item
Insulin
string
C0021641 (UMLS CUI)
67866001 (SNOMED CT 2010_0731)
MTHU002108 (LOINC Version 232)
chronic
Item
chronisch
string
C0205191 (UMLS CUI)
90734009 (SNOMED CT 2010_0731)
Allergy
Item
Allergie
string
C0020517 (UMLS CUI)
257550005 (SNOMED CT 2010_0731)
T78.40 (ICD-10-CM Version 2010)
intolerance to substance
Item
intolerance to substance
string
C1744706 (UMLS CUI)
peroxisome
Item
Peroxisom
string
C0752063 (UMLS CUI)
11191006 (SNOMED CT 2010_0731)
Fenofibrate
Item
Fenofibrate (substance)
string
C0033228 (UMLS CUI)
386879008 (SNOMED CT 2010_0731)
Metformin
Item
Metformin (substance)
string
C0025598 (UMLS CUI)
372567009 (SNOMED CT 2010_0731)
MTHU016062 (LOINC Version 232)
Actos
Item
Pioglitazone hydrochloride
string
C0872972 (UMLS CUI)
116097005 (SNOMED CT 2010_0731)
Avandia
Item
Rosiglitazone maleate
string
C0795660 (UMLS CUI)
116096001 (SNOMED CT 2010_0731)
statin
Item
Hydroxymethylglutaryl-CoA Reductase Inhibitors
string
C0360714 (UMLS CUI)
372912004 (SNOMED CT 2010_0731)
Myopathy
Item
Myopathie
string
C0026848 (UMLS CUI)
129565002 (SNOMED CT 2010_0731)
10028641 (MedDRA 13.1)
G72.9 (ICD-10-CM Version 2010)
359.9 (ICD-9-CM Version 2011)
Abnormalities, Drug-Induced
Item
Abnormalities, Drug-Induced
string
C0000771 (UMLS CUI)
Creatine Kinase
Item
Kreatin(phospho)kinase, CPK
string
C0010287 (UMLS CUI)
75828004 (SNOMED CT 2010_0731)
MTHU006937 (LOINC Version 232)
Elevated liver enzyme levels
Item
Elevated liver enzyme levels
string
C0857093 (UMLS CUI)
10014480 (MedDRA 13.1)
Neutrophil count decreased
Item
Neutropenia
string
C0853697 (UMLS CUI)
10029366 (MedDRA 13.1)
E12198 (CTCAE Version 4.03)
Creatinine abnormal
Item
Kreatinin abnormal
string
C0740471 (UMLS CUI)
10011359 (MedDRA 13.1)
Clinical Research
Item
klinische Studie
string
C0008972 (UMLS CUI)
Physical Examination
Item
Physical examination procedure
string
C0031809 (UMLS CUI)
5880005 (SNOMED CT 2010_0731)
10034986 (MedDRA 13.1)
MTHU028014 (LOINC Version 232)
89.7 (ICD-9-CM Version 2011)
Laboratory Procedures
Item
Labortest
string
C0022885 (UMLS CUI)
15220000 (SNOMED CT 2010_0731)
10059938 (MedDRA 13.1)
ECG
Item
Elektrokardiogramm (EKG)
string
C1623258 (UMLS CUI)
46825001 (SNOMED CT 2010_0731)
10014084 (MedDRA 13.1)
patient safety
Item
patient safety
string
C1113679 (UMLS CUI)

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