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Empagliflozin and Renal Oxygenation in Healthy Volunteers

Effects of the SGLT2 Inhibitor Empagliflozin on Renal Tissue Oxygenation in Non-diabetic Subjects

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03093103
Acronym
EMPA-REIN
Enrollment
45
Registered
2017-03-28
Start date
2017-03-16
Completion date
2018-12-31
Last updated
2019-07-30

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

Conditions

Nephropathy

Keywords

empagliflozin, kidney, BOLD-MRI

Brief summary

SGLT-2 inhibitors belong to a new class of hypoglycemic drugs with the unique property of decreasing blood glucose through an increase in glucosuria. These drugs inhibit the sodium glucose transporter 2 (SGLT2) expressed at the luminal membrane of the proximal tubule. SGLT-2 inhibition in type 2 diabetic subjects and in healthy volunteers shifts the threshold for renal glucose excretion to lower levels. This effect is independent from insulin. The inhibition of SGLT2 decreases HbA1C, systolic blood pressure and weight in diabetic subjects. Recently, the EMPA-REG trial demonstrated a decrease in cardiovascular mortality and renal endpoints in empagliflozin treated type 2 diabetic patients with established cardio-vascular disease. Because this novel hypoglycemic drug has unique and direct effects on renal tissue metabolism, it is important to better examine its effects on the kidney. With this study, we propose to explore the effects of empagliflozin on renal tissue oxygenation. Our hypothesis is that SGLT-2 inhibition decreases renal cortical energy requirements with consequently an increase in renal tissue oxygenation.

Detailed description

This study is a double-blind, randomized, placebo-controlled study that will examine the acute and chronic renal effects of empagliflozin in healthy volunteers. A total of 45 healthy volunteers will be included in the study: 15 normal weight, 15 overweight (BMI: 25-30kg/m2) and 15 obese (BMI\>30kg/m2) non diabetic subjects (as determined after an oral glucose tolerance test). Empagliflozin 10mg vs placebo will be administered in a blinded fashion qd. The acute and chronic renal response to empagliflozin will be assessed.

Interventions

DRUGEmpagliflozin 10 mg

Prescription of empagliflozin 10 mg once a day Follow-up of renal parameters including BOLD MRI

DRUGPlacebo

Prescription of a placebo once a day Follow-up of renal parameters including BOLD MRI

Sponsors

Centre Hospitalier Universitaire Vaudois
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Caregiver, Investigator)

Masking description

Placebo and Empagliflozin pills

Intervention model description

Randomised placebo-controlled double blind trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Normal weight (BMI: 19-24.9kg/m2), overweight (BMI:25-30kg/m2) or obesity (BMI\>30kg/m2) * Men and women (with a negative pregnancy test) during the follicular phase of the menstrual cycle. All groups will have a balanced number of men and women. * OGTT/HbA1C: normal or pre-diabetes * eGFR\>60ml/min, albumin/creatinine ratio \<3.3mg/mmol (\<30 mg/g) * Signed consent form * Normal renal ultrasound * Normal urine dipstick

Exclusion criteria

* Antihypertensive therapy * NSAID treatment * Former bariatric surgery * Age\<18y or \>50y * At risk of dehydration or hypotension * Past history of recurrent genital or urinary tract infections * Contra-indication for MR imaging (pacemaker or other implanted metallic device, claustrophobia) * Pregnancy * Sustained systolic blood pressure \>150mmHg or diastolic blood pressure \>95mmHg

Design outcomes

Primary

MeasureTime frameDescription
Renal oxygenation18 monthsThe acute and chronic effect of empagliflozin on renal oxygenation will be assessed by BOLD-MRI

Secondary

MeasureTime frameDescription
Effect of body weight on the renal response to empagliflozin18 monthsDifferent groups of BMI will be evaluated
Acute and chronic effects of empagliflozin on diurnal and nocturnal sodium, potassium, uric acid, calcium, phosphate, glucose and lithium clearances after 4 weeks treatment18 monthsWill be assessed on 24h urinary collections
Acute and chronic effects of empagliflozin on renal resistance indexes and renal volume after 4 weeks treatment18 monthsWill be assessed by renal ultrasound
Effects of empagliflozin on 24h blood pressure mesaurements18 monthsWIll be assessed by ambulatory blood pressure measurements

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026