Analysing the Effect of Empagliflozin on Reduction of Tissue Sodium Content in Patients With Chronic Heart Failure

Chronic Heart Failure Clinical Trial

— ELSI  

Official title:

Randomized, Double-blind, Placebo Controlled, Parallel-group, Prospective Clinical Study to Analyse the Effect of Empagliflozin on Reduction of Tissue Sodium Content in Patients With Chronic Heart Failure

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03128528
• Other study ID #: CRC2017ELSI
• Status: Completed
• Phase: Phase 2
• Start date: July 1, 2017
• Est. completion date: April 30, 2020

Study information

• Verified date: September 2020
• Source: University of Erlangen-Nürnberg Medical School
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The hypothesis is that the SGLT-2 inhibitor empagliflozin reduces tissue sodium content in patients with chronic heart failure, and if the hypothesis is proven, that this mechanism contributes to the beneficial effects found in EMPA-REG Outcome trial potentially via exerting beneficial effects on the vascular structure and function of the micro- and macrocirculation.

Description:

SGLT-2 inhibitors such as empagliflozin inhibit the SGLT-2 transport in the proximal tubular cells of the kidney, thereby causing glucosuria to approximately 100 g per day (and sometimes even more). The SGLT-2 inhibition does not only cause glucosuria but also natriuresis, since with each molecule of glucose one molecule of sodium is inhibited to be reabsorbed. Indeed, during the first week SGLT-2 inhibition causes clinically detectable natriuresis but its effect in the long run is not yet illustrated. Of course, a new sodium balance will be achieved after a certain time (otherwise the human body would be completely salt depleted), but total sodium content could be different. With new innovative magnetic resonance imaging (MRI) technology we are able to assess tissue sodium content in the skin and muscle, and observed that sodium content is significantly increased with aging, severe hypertension or hyperaldosteronism. Furthermore, skin sodium content assessed by MRI was closely related to left ventricular mass (r=0.559, p<0.0001, N=89) independently of age, gender, body mass index, and 24 h ambulatory blood pressure (β=0.343, p=0.001, N=89) 11. Using this technology, our first yet unpublished data (clinicaltrials.gov: NCT02383238) indicate that SGLT-2 inhibition decreases sodium content in the skin in patients with diabetes. Finally, we observed previously that in patients with acute chronic heart failure skin sodium content decreased from 43.5 mmol/l to 32.2 mmol/l after diuretic therapy.

Thus, the present study aims at analyzing changes in total and tissue sodium content after SGLT-2 inhibition with empagliflozin. In parallel, sodium intake and excretion and central systolic and pulse pressure as well as other vascular parameters will be assessed. In face of the upcoming studies with empagliflozin conducted in patients with reduced and preserved ejection fraction (two large-scale, prospective, doubleblind, placebo controlled studies planned by Boehringer Ingelheim as the sponsor), we thought that we focus on patients with chronic heart failure irrespective diabetic status. The hypothesis is that the SGLT-2 inhibitor empagliflozin reduces tissue sodium content in patients with chronic heart failure, and if the hypothesis is proven, that this mechanism contributes to the beneficial effects found in EMPA-REG Outcome trial potentially via exerting beneficial effects on the vascular structure and function of the micro- and macrocirculation.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 84
• Est. completion date: April 30, 2020
• Est. primary completion date: January 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Age of 18 - 85 years

• Male and Female patients (females of child bearing potential must be using adequate contraceptive precautions)

• CHF (symptoms and/or sign of CHF, ejection fraction < 40% (HfrEF) 14 or symptoms and/or signs of CHF, ejection fraction 40-49 % and NT-pro BNP > 125 pg/ml, and at least one structural abnormality of left atrium or ventricle (HFmEF) 14 in stable conditions.

• Females of childbearing potential or within two years of the menopause must have a negative urine pregnancy test at screening visit.

• Informed consent has to be given in written form.

Exclusion Criteria:

• Any other form of diabetes mellitus than type 2 diabetes mellitus

• Use of insulin or any SGLT-2 inhibitor within the past 10 weeks prior to the screening visit (visit 1).

• Patients with more than two blood glucose lowering medications

• Uncontrolled diabetes (fasting plasma glucose = 240 mg/dl, HbA1c = 10%)

• Any history of stroke, transient ischemic attack, instable angina pectoris, or myocardial infarction within the last 6 months prior to study inclusion

• Estimated glomerular filtration rate (eGFR) < 30 ml/min/1.73m² (following the inclusion criteria of EMPA-REG OUTCOME study 1-3)

• Chronic heart failure NYHA stage IV

• Use of loop diuretics above furosemide > 80 mg/day, or torasemide >40 mg/day, or piretanide > 6 mg/day

• Implanted pacemakers or defibrillators

• Any other relevant clinical contraindication of MRI examination

• Uncontrolled arterial hypertension (i.e. = 180/110 mmHg)

• Severe disorders of the gastrointestinal tract or other diseases which interfere with the pharmacodynamics and pharmacokinetics of study drugs

• Significant laboratory abnormalities such as Serum Glutamate-Oxaloacetate-Transaminase (SGOT) or Serum Glutamate-Pyruvate-Transaminase (SGPT) levels more than 3 x above the upper limit of normal range

Related Conditions & MeSH terms

• Chronic Heart Failure
• Heart Failure

Intervention

Drug:
• Empagliflozin 10mg
Each patient, after the run-in/wash-out phase, will be randomly assigned in a doubleblind fashion to one of the two treatment sequences according to a randomisation list. and provided by the sponsor.
• Placebo Oral Tablet
Each patient, after the run-in/wash-out phase, will be randomly assigned in a doubleblind fashion to one of the two treatment sequences according to a randomisation list. and provided by the sponsor.

Locations

Country	Name	City	State
Germany	Clinical Research Center, Department of Nephrology and Hypertension, University of Erlangen-Nuremberg	Erlangen

Sponsors (1)

Lead Sponsor	Collaborator
University of Erlangen-Nürnberg Medical School

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Striepe K, Jumar A, Ott C, Karg MV, Schneider MP, Kannenkeril D, Schmieder RE. Effects of the Selective Sodium-Glucose Cotransporter 2 Inhibitor Empagliflozin on Vascular Function and Central Hemodynamics in Patients With Type 2 Diabetes Mellitus. Circulation. 2017 Sep 19;136(12):1167-1169. doi: 10.1161/CIRCULATIONAHA.117.029529. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Skin sodium content	Skin sodium content (23Na-MRI) assessed at the lower leg	14 weeks
Secondary	Muscle sodium content	Sodium content of muscles	14 weeks
Secondary	Water content of skin and muscle	Water content (1H) of skin and muscle	14 weeks
Secondary	Sodium excretion	Sodium excretion as assessed by sodium creatinine ratio in spot urine	14 weeks
Secondary	24-hour urine sodium excretion	24-hour urine sodium excretion	14 weeks
Secondary	Vascular stiffness Parameter (central systolic pressure)	Vascular stiffness Parameter under resting conditions and ambulatory conditions and their association to change in tissue sodium content	14 weeks
Secondary	Flow mediated vasodilation	Flow mediated vasodilation (FMD) as measured by semiautomated ultrasound system	14 weeks
Secondary	N-terminal prohormone of brain natriuretic peptide	N-terminal prohormone of brain natriuretic peptide (NT-pro-BNP) to assess their relation to change in tissue sodium content	14 weeks
Secondary	Body weight	Measurement of body weight in kg	14 weeks
Secondary	HbA1c	Diabetic control (e.g. fasting glucose, glycosylated hemoglobin [HbA1c])	14 weeks
Secondary	ABPM	24-hour ambulatory blood pressure (ABP)	14 weeks
Secondary	Visual analogue scale for dyspnea	Visual analogue scale for dyspnea to assess their relation to change in tissue sodium Content.	14 weeks
Secondary	Body constitution	Body constitution (fluid status based on three compartment model lean body mass, adipose tissue mass and overhydration)	14 weeks
Secondary	Vascular stiffness Parameter (Pulse pressure)	Vascular stiffness Parameter under resting conditions and ambulatory conditions and their association to change in tissue sodium content	14 weeks