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Metformin Pharmacokinetics in Patients With Chronic and Acute Heart Failure

Metformin in Patients With Chronic and Acute Heart Failure: Pharmacokinetics and Polymorphisms in Genes Encoding Membrane Metformin Transporter Proteins

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02797340
Acronym
MetKin
Enrollment
110
Registered
2016-06-13
Start date
2016-01-11
Completion date
2018-04-30
Last updated
2018-04-20

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

Conditions

Heart Failure, Systolic

Brief summary

The study evaluates the pharmacokinetics of metformin in heart failure patients in acute and chronic state in relation to metformin transporter genotypes. Participants have heart failure and type 2 diabetes treated with metformin. Hypothesis: Primary: The renal clearance of metformin is decreased in acute state of congestive heart failure compared with chronic state. Secondary: Metformin trough values in HF patients are influenced by polymorphisms in transporter genes relevant to the pharmacokinetics of metformin.

Detailed description

Background: Heart failure (HF) is a common disease and diabetes/insulin resistance are present in approximately 50 % of HF patients. Metformin is the most commonly prescribed oral anti-diabetic drug, and a huge inter-individual variability in trough steady-state metformin concentration in type 2 diabetics have been demonstrated. Genetic polymorphisms in metformin transporter genes are likely to have a direct impact on metformin pharmacokinetics and variability in drug responses, but the influence of polymorphisms in these transporter genes on circulating metformin levels is presently unknown in HF patients. Objectives: A) To compare the pharmacokinetics of metformin in 12 diabetic patients with HF in acute and chronic state. B) To investigate the influence of polymorphisms in genes encoding the metformin transporter proteins on metformin trough levels in 150 diabetic HF patients. Design: An open, single-center study enrolling 12 patients with acute heart failure (study A) and 150 patients with stable chronic heart failure (study B). The participants have diabetes already treated with metformin prior to inclusion. Through repeated blood draws, the concentration of metformin will be determined along with genotyping for metformin transporter genes. Primary outcome: Study A: Changes in renal clearance of metformin between patients with acute and chronic heart failure. Study B: Mean trough steady-state concentrations of metformin with emphasis on the intra-interindividual variability in HF patients.

Interventions

OTHERBlood draws and urine samples for metformin concentration measurements
DRUGMetformin

Sponsors

Aarhus University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with heart failure * LVEF \< 45% within 12 months prior to inclusion * NYHA-class I, II, III or IV * Ability to understand the written patient information and to give informed consent * Diabetes Type 2 (and in metformin treatment for \> 1 month) * Stable dosage of metformin treatment for at least 1 week prior to examination

Exclusion criteria

* Age \< 18 years * Current abuse of alcohol or drugs

Design outcomes

Primary

MeasureTime frame
Changes in renal clearance of metformin between patients with acute and chronic heart failure.approximately 2 weeks
Mean trough steady-state concentrations of metformin with emphasis on the intra-interindividual variability in HF patients3 weeks

Countries

Denmark

Outcome results

None listed

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