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NCT Number: NCT06435858

Short-term Effects of an SGLT2 Inhibitor on Divalent Ions in Autosomal Dominant Polycystic Kidney Disease

This study aims to better understand electrolyte handling in patients with autosomal dominant polycystic kidney disease treated with the SGLT2 inhibitor Empagliflozin.

Patients will be randomized into two groups and take Empagliflozin or a Placebo for 2 weeks with a wash-out period of 2 weeks. The primary outcome is tubular handling of the divalent ions calcium, phosphate and magnesium. Secondary outcomes include diuresis, safety and tolerability.

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University Hospital Zurich, Division of Nephrology, Zurich, Canton of Zurich, Switzerland

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About this study

This investigator-initiated randomised, single-blind, placebo-controlled cross-over study aims to better understand tubular electrolyte handling of divalent ions in patients with autosomal dominant polycystic kidney disease treated with the SGLT2 inhibitor Empagliflozin.

After randomization, at week 0, participants collect 24-hour urine sample and a patient visit to assess vitals and blood tests takes place. After this visit, period 1 starts with a 2-week treatment of either Empagliflozin 10mg or Placebo.

At week 2, the second 24-hour-urine sample and 2. patient visit and blood test take place. After this visit, wash-out period for 2 weeks starts where no study drug will be administered At week 4, the period 2, the crossover-period starts for an additional 2 weeks. At week 6; a final and third 24-hour urine sample, clinical visit and blood test takes place.

At week 3 & 7, a phone consultation will assess safety.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • - Patients 18-75 years old with ADPKD, defined according to international diagnostic and classification criteria14, treated at Cantonal Hospital Graubünden (KSGR) and the University Hospital Zürich (USZ) independent of baseline treatment with the vasopressin receptor antagonist Tolvaptan
  • Informed consent as documented by signature

Exclusion criteria

  • - renal replacement therapy or kidney allograft recipient
  • chronic kidney disease CKD KDIGO Stage G4 (eGFR under 30ml/min/1.73m2)
  • patients younger 18 years of age
  • Diabetes mellitus type 1
  • recurrent urinary tract infections (UTI) defined as more than 3 infections requiring antibiotic treatment or over 1 requiring hospitalization/year.
  • Patients with uncontrolled hypertension (defined as ambulatory systolic BP over 180mmHg), liver cirrhosis (Child Pugh B and C)
  • Patients not able or not willing to stop the following medications during the study period of participation in the trial:
  • Thiazide diuretics
  • Carbonic anhydrase inhibitors
  • Sodium bicarbonate
  • 1, 25 (OH) vitamin D (calcitriol)
  • Bisphosphonate, denosumab, teriparatide
  • Pregnant or lactating women
  • Known allergy to study drug
  • Inability to understand and follow the protocol

Treatment and study plan

Empagliflozin

Drug

Empagliflozin 10mg

Placebo

Drug

Placebo capsule

Primary outcomes

  1. Primary Outcome

    Time frame: After a two week intervention

    • Calcium, phosphate, magnesium excretion

Secondary outcomes

  1. Secondary Outcome

    Time frame: After a two week intervention

    • diuresis (24-hour urine volume, 24-hour creatinine, ketonuria, osmolarity, urinary pH) - tubular handling of other electrolytes (Na, K, Cl) - inflammation metabolism (CRP, hemoglobin?) - kidney function (creatinine, uric acid, urea, hemoglobin?) - effect on standardized blood pressure (assessed every two weeks) - bone metabolism (FGF23, PTH, 25-(OH)-D3) - tolerability (patient-reported side effects (nycturia, urinary urgency, lightheadedness, syncope) - safety (bacteriuria, urinary tract infection requiring antibiotic treatment, genital mycosis)

Study contacts

Contact information is provided by the study sponsor or research team.

Patrick Hofmann, MD

CONTACT

[email protected]

+4181 256 6305

Thomas Fehr, MD

CONTACT

[email protected]

+4181 256 6305

Sponsors and collaborators

Lead sponsor

Cantonal Hospital Graubuenden

Other

Collaborators

  • University of Zurich

Registry information

Acronym: SIDIA

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
May 30, 2024
Registry last updated
Sep 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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