MetKin: Metformin Pharmacokinetics in Patients With Chronic and Acute Heart Failure

Sponsor
Aarhus University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02797340
Collaborator
(none)
110
1
1
27.6
4

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Blood draws and urine samples for metformin concentration measurements
  • Drug: Metformin
Phase 4

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:
  1. To compare the pharmacokinetics of metformin in 12 diabetic patients with HF in acute and chronic state.

  2. 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
110 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Metformin in Patients With Chronic and Acute Heart Failure: Pharmacokinetics and Polymorphisms in Genes Encoding Membrane Metformin Transporter Proteins
Actual Study Start Date :
Jan 11, 2016
Anticipated Primary Completion Date :
Apr 30, 2018
Anticipated Study Completion Date :
Apr 30, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Interventional

All participants

Other: Blood draws and urine samples for metformin concentration measurements

Drug: Metformin

Outcome Measures

Primary Outcome Measures

  1. Changes in renal clearance of metformin between patients with acute and chronic heart failure. [approximately 2 weeks]

  2. Mean trough steady-state concentrations of metformin with emphasis on the intra-interindividual variability in HF patients [3 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aarhus University Hospital, Department of Cardiology, Palle Juul-Jensens Boulevard 99 Aarhus N Denmark 8200

Sponsors and Collaborators

  • Aarhus University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Henrik Wiggers, Senior consultant, associate professor, PhD, DMSc, Aarhus University Hospital
ClinicalTrials.gov Identifier:
NCT02797340
Other Study ID Numbers:
  • 50268-20150921
First Posted:
Jun 13, 2016
Last Update Posted:
Apr 20, 2018
Last Verified:
Apr 1, 2018
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 20, 2018