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Study identifier: NCT04447911 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effects of the SGLT2 Inhibitor Empagliflozin in Patients With Euvolemic and Hypervolemic Hyponatremia

Condition: Hyponatremia · SIADH · Liver Failure  ·  Sponsor: University Hospital, Basel, Switzerland

PhasePhase 4
Planned participants172
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Hyponatremia is the most common electrolyte derangement occurring in hospitalized patients. It is usually classified as hypovolemic, euvolemic or hypervolemic. The most common aetiology of euvolemic hyponatremia is the syndrome of inappropriate antidiuresis (SIAD). Hypervolemic hyponatremia is common in patients with congestive heart failure (CHF) (10-27%) and liver cirrhosis (up to approximately 50%). In SIAD, the regulation of arginine vasopressin (AVP) secretion is impaired which leads to free water retention. In CHF and liver cirrhosis, the effective arterial blood volume is decreased leading to non-osmotic baroreceptor mediated AVP release and consecutive free water retention. Current treatments of euvolemic and hypervolemic hyponatremia, including the most used treatment fluid restriction, are of limited efficacy. Sodium-Glucose-Co-Transporter 2 (SGLT2) inhibitors reduce glucose reabsorption in the proximal tubule, resulting in glucosuria and consecutive osmotic diuresis. A placebo-controlled randomized trial of our group has shown that a short-term, i.e. a 4-days administration of the SGLT2 inhibitor empagliflozin (Jardiance)® in addition to fluid restriction was effective in increasing the serum sodium concentration in 87 patients with SIAD-induced hyponatremia. The effect of empagliflozin (Jardiance)® without additional fluid restriction is however not yet known. Large randomized controlled trials have shown that SGLT2 inhibitors reduced hospitalization for heart fa…

This description comes directly from the study's public registry record.

Talk to the study team

Mirjam Christ-Crain, Prof  ·  +41 61 328 70 80  ·  Mirjam.Christ-Crain@usb.ch

Always discuss trial participation with your own doctor first.

Locations (6)

University Hospital of Würzburg, med. PoliklinikWürzburg, GermanyRecruiting
Erasmus Universität Medisch Centrum Rotterdam, Department of Internal MedicineRotterdam, NetherlandsRecruiting
Centre Hospitalier Universitaire Vaudois (CHUV)Lausanne, Canton of Vaud, SwitzerlandRecruiting
University Hospital BaselBasel, SwitzerlandRecruiting
Spitalzentrum BielBiel, SwitzerlandRecruiting
Kantonsspital LuzernLucerne, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT04447911