Skip to content

Metformin Reduces Left Ventricular Mass in Patients With Ischemic Heart Disease

Metformin Reduces Left Ventricular Mass in Patients With Ischemic Heart Disease:A Randomized, Double-Blind, Placebo-Controlled Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01879293
Enrollment
120
Registered
2013-06-17
Start date
2013-07-31
Completion date
2015-08-31
Last updated
2015-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Left Ventriclar Mass

Keywords

Metformin, Left ventricular mass, Endothelial dysfunction, cardiac magnetic resonance, aortic pulse wave

Brief summary

Cardiovascular disease is the most common cause of death in the world. Most of the attention in treating ischemic heart disease (IHD) is understandably directed toward treating coronary artery disease. However there are other treatable culprits in these patients. Left ventricular hypertrophy (LVH) is widespread in IHD patients, even in the absence of hypertension. It is a strong predictor of cardiovascular events and all-cause mortality. In one study, the presence of LVH was a stronger predictor of mortality than either multivessel cor-onary disease or impaired LV function. Metformin is an antihyperglycemic agent with a history of successful use in type 2 diabetes. In the UKPDS (United Kingdom Prospective Diabetes Study), metformin was associated with a 39% lower risk of myocardial infarction compared with conventional therapy. Metformin also offered dual benefits of improving vascular function and lessening ischemia in nondiabetic patients. Hence, the main aim of this study was to assess whether metformin could regress LVM in patients with IHD. The secondary aim was to assess the effect of metformin on LV volumes and endothelial function in this patient group.

Interventions

DRUGMetformin
DRUGplacebo

Sponsors

Wuhan General Hospital of Guangzhou Military Command
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* They had to have normal glucose tolerance. * They had to have either angiographically documented coronary artery disease or a previous history of myocardial infarction. * They were required to have an office BP \< 130/80 mm Hg * The presence of LVH on echocardiography (American Society of Echocardiography criteria LVM index \[LVMI\] \> 115 g/m2 for men and \> 95 g/m2 for women).

Exclusion criteria

* They were currently prescribed metformin. * They had renal and liver dysfunction, heart failure, or malignancy, or were unable to give informed consent. * Patients with contraindications to cardiac magnetic resonance (CMR) (pacemakers, claustrophobia) were also excluded, as were pregnant or lactating women.

Design outcomes

Primary

MeasureTime frameDescription
Left ventricular mass.one yearWe will measure left ventricular mass before and after metformin intervention with cardiac magnetic resonance.

Secondary

MeasureTime frameDescription
Left ventricular volume and endothelial function.one yearWe measure the left ventricular volume and endothelial function before and after metformin intervention by cardiac magnetic resonance and high resolution ultrasound.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026