Age
Item
aged 18 years or over
boolean
C0001779 (UMLS CUI [1])
Informed consent
Item
participant willing and able to give informed consent.
boolean
C0021430 (UMLS CUI [1])
Ischaemic heart disease | Coronary heart disease angiogram | History of myocardial infarction | H/O: angina pectoris
Item
documented ischaemic heart disease: either angio-graphically documented coronary artery disease or a previous history of myocardial infarction/angina.
boolean
C1869045 (UMLS CUI [1])
C0010068 (UMLS CUI [2,1])
C0002978 (UMLS CUI [2,2])
C1275835 (UMLS CUI [3])
C0455530 (UMLS CUI [4])
Left Ventricular Hypertrophy Echocardiography | Gender
Item
screening echocardiography based diagnosis of lvh based on ase criteria (males >115g/m2, females >95g/m2)
boolean
C0149721 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
C0079399 (UMLS CUI [2])
Fasting insulin measurement Resistance.index | Glycosylated hemoglobin A
Item
fasting insulin resistance index ≥ 2.7 and/or hba1c >5.6 and less than 6.5 at screening
boolean
C2016107 (UMLS CUI [1,1])
C0807745 (UMLS CUI [1,2])
C0019018 (UMLS CUI [2])
Blood Pressure | 24 hour blood pressure
Item
blood pressure < 140/85 mm hg or 24hr bp <135/85 daytime average in screening
boolean
C0005823 (UMLS CUI [1])
C1282173 (UMLS CUI [2])
Compliance behavior Study Protocol
Item
able (in the investigators opinion) and willing to comply with all study requirements.
boolean
C1321605 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
Impaired cognition
Item
cognitive impairment
boolean
C0338656 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
type 1 or 2 diabetes mellitus
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
Chronic heart failure Echocardiography
Item
chronic heart failure as evidenced by echocardiogram or documented diagnosis of chf
boolean
C0264716 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
Left ventricular ejection fraction Echocardiography
Item
left ventricular ejection fraction <45% on screening echocardiography
boolean
C0428772 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
Medical contraindication Magnetic Resonance Imaging (MRI) of Heart | Artificial cardiac pacemaker | Claustrophobia | Presence of metallic device / implant | Eye Injuries, Penetrating | Eye Exposure to Retained metal fragments
Item
contraindications to cardiac mri (pacemakers, claustrophobia, metal implants, history of penetrative eye injury or exposure to metal fragments in eye requiring medical attention)
boolean
C1301624 (UMLS CUI [1,1])
C0412692 (UMLS CUI [1,2])
C0030163 (UMLS CUI [2])
C0008909 (UMLS CUI [3])
C3693688 (UMLS CUI [4])
C0015409 (UMLS CUI [5])
C0015392 (UMLS CUI [6,1])
C0332157 (UMLS CUI [6,2])
C2921327 (UMLS CUI [6,3])
Malignant Neoplasms Therapeutic procedure | Life-threatening disease | Kidney Diseases | Chronic Kidney Diseases
Item
malignancy (receiving active treatment) or other life threatening disease, renal disease (ckd class 3b or worse)
boolean
C0006826 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C3553594 (UMLS CUI [2])
C0022658 (UMLS CUI [3])
C1561643 (UMLS CUI [4])
Pregnancy | Breast Feeding
Item
pregnancy/lactating females
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Indication of Inappropriate
Item
any other reason considered inappropriate by a study physician
boolean
C0392360 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
Study Subject Participation Status
Item
participants who have participated in any other clinical trial within the previous 30 days.
boolean
C2348568 (UMLS CUI [1])