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Acute Kidney InjuryPhase 4MERCURI-2NCT05590143

proMoting Effective Renoprotection in Cardiac sURgery Patients by Inhibition of SGLT-2

A Phase 4 study testing Dapagliflozin 10 MG Oral Tablet [Farxiga] in people with Acute Kidney Injury and Cardiac Surgery, run by Amsterdam UMC at 6 sites in Netherlands.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

Multi-centre, triple-blinded (patients, physicians, investigators), parallel-group, balanced (1:1), stratified (sex, type 2 diabetes mellitus), randomized, controlled (placebo), phase IV clinical trial to investigate the potential of preoperative initiation (from day 1 before surgery) and perioperative continuation… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Dapagliflozin 10 MG Oral Tablet [Farxiga]
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
784 participants
Where
6 sitesNetherlands
Study dates
9 Jun 2023to Sep 2025
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • > 18 years-old
  • Undergoing elective cardiac surgery.
  • Providing informed consent

Who cannot join

  • Current treatment with SGLT2 inhibitors
  • Reduced kidney function at baseline with eGFR < 20 ml/min at time of inclusion
  • Diabetes Mellitus Type 1
  • History of diabetic keto acidosis
  • Diabetes Mellitus Type 2 with BMI<25 for people with type 2 diabetes who are using multiple daily insulin injections (both short and long-acting insulin)
  • Systolic blood pressure < 100 mmHg at time of inclusion
Show all 9Show fewer
  • Emergency surgery, defined as in need of surgery for medical reasons < 7 days, i.e. "S1-4" according to the Amsterdam UMC classification
  • Female of child-bearing potential who is pregnant, breast-feeding or intend to become pregnant or is not using adequate contraceptive methods
  • Known or suspected allergy to trial products or other drugs in the same class

Trial locations and contacts

6 sites in 1 country.

6 sites in 1 country

Netherlands6 sites
  • OLVG

    Amsterdam, 1090 HM

  • Amsterdam UMC

    Amsterdam, 1105 AZ

  • Amphia Hospital

    Breda, 4818 CK

  • Medisch Spectrum Twente

    Enschede, 7500 KA

  • Leiden University Medical Center

    Leiden, 2300 RC

  • St Antonius Hospital

    Nieuwegein, 3430 EM

Other trials in Netherlands

About this study

Official title: Preoperative Sodium Glucose Cotransporter 2 Inhibitors for Prevention of Postoperative Acute Kidney Injury in Cardiac Surgery Patients - a Randomized, Placebo-controlled, Multi-centre, Phase IV Clinical Trial

Multi-centre, triple-blinded (patients, physicians, investigators), parallel-group, balanced (1:1), stratified (sex, type 2 diabetes mellitus), randomized, controlled (placebo), phase IV clinical trial to investigate the potential of preoperative initiation (from day 1 before surgery) and perioperative continuation (until day 2 after surgery) of the SGLT2 inhibitor dapagliflozin 10 mg once daily to prevent AKI according to the KDIGO criteria (an increase in serum creatinine by 0.3 mg/dl (26.5 mmol/l) within 48 hours; or an increase in serum creatinine to 1.5 times baseline, within 7 days; or a urine output <0.5 ml/kg/h for >6 hours) in adult (>18 years old) patients undergoing cardiopulmonary bypass surgery.

Read the detailed description

Background of the study:

Acute kidney injury is one of the most common complications after cardiac surgery. The new glucose-lowering therapy, sodium glucose transport protein 2 inhibitors (SGLT2i) possess renoprotective properties in people with chronic kidney disease in the presence or absence of type 2 diabetes. Large cardiovascular outcome trials in patients with diabetes observed a lower incidence of acute kidney injury. However, these studies were not powered to investigate this nor did acute kidney injury concern an adjudicated endpoint.

Objective of the study:

To investigate the potential of preoperative initiation (from day 1 before surgery) and perioperative continuation (until day 2 after surgery) of the SGLT2 inhibitor dapagliflozin 10 mg once daily to prevent AKI according to the KDIGO criteria in patients undergoing cardiopulmonary bypass surgery.

Study design:

Multi-centre, triple-blinded (patients, physicians, investigators), parallel-group, balanced (1:1), stratified (sex, type 2 diabetes mellitus), randomized, controlled (placebo), phase IV clinical trial.

Study population:

Patients undergoing cardiac surgery, aged >18 years-old.

Intervention:

Participants receive 10 mg dapagliflozin once daily or matching placebo starting 1 day prior to surgery and continued until two days postoperatively (four doses).

Primary outcome of the study:

Incidence of AKI occurring in 7 days after surgery, according to KDIGO criteria, defined as an increase in serum creatinine by 0.3 mg/dl (26.5 mmol/l) within 48 hours; or an increase in serum creatinine to 1.5 times baseline, within 7 days; or a urine output <0.5 ml/kg/h for >6 hours.

Secondary outcomes of the study:

  1. Incidence of Stage 3 AKI.
  2. Postoperative change of eGFR.
  3. Postoperative Atrial Fibrillation for which treatment is initiated.
  4. Length of Stay in the Intensive Care Unit.
  5. Length of Stay in hospital.
  6. MAKE: Major Adverse Kidney Events
  7. MACE: Major Adverse Cardiovascular Events
  8. Patient-reported quality of recovery 1: DAH30: Days at Home in first 30 days
  9. Patient-reported quality of recovery 2: WHO-DAS 2.0: World Health Organisation Disability Assessment Schedule 2.0
  10. Patient-reported quality of recovery 3: EQ5D5L: 5 level EuroQol 5D questionnaire.
  11. Safety outcomes: incidence of genital mycotic infections, diabetic keto-acidosis, hypoglycaemia, postoperative complications and Serious Adverse Events (SAEs).
  12. Productivity costs
  13. Healthcare costs
  14. Hyperglycaemia (> 10 mmol/l)
  15. Hypoglycaemia (< 4 mmol/l)
  16. Heart Rate
  17. Mean Arterial Pressure
  18. Cardiac Output
  19. Peak postoperative Troponin
  20. Peak postoperative CK-MB
  21. Postoperative Left Ventricular Function
  22. Urinary oxygenation (patients included at Amsterdam UMC only)

Nature and extent of the burden and risks associated with participation, benefit and group relatedness:

General trial-related burden:

The investigators will withdraw 4.5 mL of blood at one day before surgery and one day postoperatively for biomarker analysis. No extra venepunctures are required, as these measurements coincide with routine clinical care.

Intervention group-related burden:

Participants will be asked to take either 1 tablet of 10 mg dapagliflozin once daily from 1 days before surgery until 2 days postoperative (including the day of surgery, four doses total) or a matching placebo regimen. Patients randomized to dapagliflozin will run a small risk of treatable side effects related to the study drug. These are rare for short-term treatments. Participants will be informed about the following side effects:

  1. Genital mycotic infections: these usually only occur after longer-term use of SGLT2 inhibitors. In this study, patients will only receive this medication for up to 10 doses. Treatment of this side effect is straightforward with antifungal treatment.
  2. Euglycemic ketoacidosis: a lowering of the pH in the blood through the build-up of ketones. This has been described in patients on long-term treatment and is ascribed to altered insulin sensitivity through increased glucose loss by SGLT2 inhibition. For this and other reasons, patients with type 1 diabetes mellitus and patients with type 2 diabetes mellitus and a body mass index <25 kg/m2 are excluded from this trial. We will monitor perioperative glucose and pH levels in all participants according to routine perioperative care. In addition, patients using insulin therapy will receive a perioperative glucose/insulin infusion, which suppresses ketone production. Should keto acidosis occur in any other patient, treatment is straightforward with a glucose-insulin infusion.
  3. Hypoglycemia: only patients with diabetes mellitus using sulfonylurea or insulin are at risk, according to previous research. To prevent this side effect: patients will receive an individualized adaptation of their glucose-lowering medication by the investigator team. To treat this side effect, blood glucose will be monitored in all patients according to standard perioperative cardiac surgery care and hypoglycaemia treatment protocols with urgent administration of intravenous glucose are in place.

Risk-benefit:

There is solid evidence to support that SGLT2 inhibitors offer kidney protection. Acute kidney injury is a common complication after cardiac surgery. The investigator's hypothesis is, therefore, that patients in the intervention group will receive protection against acute kidney injury. In addition, the results from this trial could lead to the improvement of care and protection of future patients undergoing cardiac surgery. The side-effect profile of dapagliflozin is mild, and participants will be intensively monitored in this study. Therefore, the investigators estimate that the benefits outweigh the risks of participation in this trial.

Relevance and intended applications:

The aim of this study is to determine whether SGLT2i can reduce the incidence of AKI following cardiac surgery. Based on the results of this trial, SGLT2 inhibitors can be applied as a standard prophylactic treatment in cardiac surgery patients to prevent AKI.

Sample size:

The investigators expect an incidence of AKI in the placebo group of 22%, as a conservative estimation, based on previous cohorts. Large outcome trails found a relative risk reduction for AKI of 0.64 with SGLT2 inhibition. This translates into an absolute risk reduction of 7.9% and an expected incidence in the intervention group of 14.1%. The required total sample size to find such a difference based on Fisher Exact test, with two-sided alpha at 0.05 and 80% power is 784. Therefore, the aim is to include 392 patients per arm.

Keywords: SGLT2i; Acute Kidney Injury (AKI); Cardiac Surgery

Being tested
Dapagliflozin 10 MG Oral Tablet [Farxiga], Placebo
Keywords
Cardiac Surgery, Acute Kidney Injury, SGLT2i, Dapagliflozin
Medical subject headings
Acute Kidney Injury

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Dapagliflozin 10 MG Oral Tablet [Farxiga]Drug

    Also called Farxiga, SGLT2i, Sodium glucose co-transporter-2 inhibitor

    One oral tablet, once daily starting one day prior to surgery and continued until two days postoperatively (four doses).

  • PlaceboDrug

    One oral tablet, once daily starting one day prior to surgery and continued until two days postoperatively (four doses).

Study groups in NCT05590143
Study groupRoleWhat they receive
InterventionExperimentalDapagliflozin 10 mg
Receives: Drug: Dapagliflozin 10 MG Oral Tablet [Farxiga]
PlaceboPlacebo comparatorMatching Placebo
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. AKI

    Incidence of Acute Kidney Injury (AKI) occurring in 7 days after surgery, according to KDIGO criteria, defined as an increase in serum creatinine by 0.3 mg/dl (26.5 mmol/l) within 48 hours; or an increase in serum creatinine to 1.5 times baseline, within 7 days; or a urine output <0.5 ml/kg/h for >6 hours.

    Measured: Recorded daily until day 7 postoperatively or until discharge from hospital (earlier).

Secondary outcomes (22)
  1. AKI-3

    Incidence of Stage 3 AKI according to KDIGO (Kidney Disease Improving Globel Outcomes) criteria.

    Measured: Recorded daily until day 7 postoperatively or until discharge from hospital (earlier).

  2. eGFR

    Postoperative maximum change of estimated Glomerular Filtration Rate (eGFR) compared to the baseline eGFR.

    Measured: Recorded daily until day 7 postoperatively or until discharge from hospital (earlier).

  3. AF

    Postoperative Atrial Fibrillation (AF) defined as any episode for which treatment is initiated.

    Measured: Recorded daily until day 7 postoperatively or until discharge from hospital (earlier).

  4. LoS-ICU

    Length of Stay in the Intensive Care Unit (LoS-ICU), measured in days from transfer to ICU.

    Measured: Recorded on day of discharge from ICU, assessed up to 30 days.

  5. LoS-Hos

    Length of Stay in the Hospital, measured in days from admission to hospital.

    Measured: Recorded on day of discharge from the hospital, assessed up to 30 days.

  6. MAKE

    Major Adverse Kidney Events (MAKE). Composite endpoint of death, new dialysis, and worsened renal function.

    Measured: Within 30 days postoperatively.

  7. MACE

    Major Adverse Cardiovascular Events (MACE). Composite endpoint of cardiovascular death, nonfatal myocardial infarction (MI), nonfatal ischaemic cerebral vascular accident (iCVA) and hospitalization for heart failure.

    Measured: Within 30 days postoperatively.

  8. QoR 1: DAH30

    Patient-reported quality of recovery, according DAH30: Days at Home in first 30 days.

    Measured: Recorded at 30 days postoperatively.

  9. QoR 2: WHODAS2

    Patient-reported Quality of Recovery (QoR), according to World Health Organisation Disability Assessment Schedule 2.0 (WHO-DAS2.0). Summarized in a score between 0 - 100 with 0 being the best score (no disability) and 100 the worst (maximal disability).

    Measured: Recorded at 30 days postoperatively.

  10. QoR 3: EQ5D5L

    Patient-reported Quality of Recovery (QoR), according to 5 level EuroQol 5D questionnaire (EQ5D5L): a standardised measure of health status developed by the EuroQol Group to provide a simple, generic measure of health for clinical and economic appraisal. Summarized in a score between 0 - 1 with 0 being the best score (no disability) and 1 the worst (maximal disability).

    Measured: Recorded at 30 days postoperatively.

  11. Safety outcomes

    Genital mycotic infections, diabetic keto-acidosis, and hypoglycaemia, in addition to incidence of postoperative complications and Serious Adverse Events (SAEs)

    Measured: Within 30 days postoperatively.

  12. Health care costs

    Healthcare costs will be objectified to weigh cost-effectiveness, using the iMCQ:

    • IMCQ: IMTA (Institute for Medical Technology Assessment) Medical Consumption Questionnaire

    Measured: Recorded at 30 days postoperatively.

  13. Productivity costs

    Productivity costs will be objectified to weigh cost-effectiveness, using the iPCQ: IMTA (Institute for Medical Technology Assessment) Productivity Cost Questionnaire

    Measured: Recorded at 30 days postoperatively.

  14. Hypoglyceamia

    Incidence of hypoglycaemia (blood glucose < 4 mmol/l) detected during routine peri-operative glucose measurements.

    Measured: From admission to hospital until day 3 postoperatively.

  15. Hyperglyceamia

    Incidence of hyperglycaemia (blood glucose > 10 mmol/l) detected during routine peri-operative glucose measurements.

    Measured: From admission to hospital until day 3 postoperatively.

  16. Haemodynamics 1: HR

    Peri-operative hourly average heart rate (HR, beats per minute) from the start of anaesthesia until discharge from the Intensive Care Unit.

    Measured: From start of anaesthesia until discharge from the Intensive Care Unit, assessed up to 72 hours.

  17. Haemodynamics 2: MAP

    Peri-operative hourly average mean arterial blood pressure (MAP, mmHg) from start of anaesthesia until discharge from the Intensive Care Unit.

    Measured: From start of anaesthesia until discharge from the Intensive Care Unit, assessed up to 72 hours.

  18. Haemodynamics 3: CO

    Peri-operative average hourly cardiac output (CO, l/min) from start of anaesthesia until discharge from the Intensive Care Unit.

    Measured: From start of anaesthesia until discharge from the Intensive Care Unit, assessed up to 72 hours.

  19. Cardiac biomarker 1: Troponin

    Peak troponin concentration, routinely measured during clinical practice.

    Measured: From transfer to ICU until 48 hours postoperatively.

  20. Cardiac biomarker 2: CK-MB

    Peak CK-MB concentration, as routinely measured during clinical practice.

    Measured: From transfer to ICU until 48 hours postoperatively.

  21. Postoperative LVF

    Qualitative assessment (categorised as normal, or mildly, moderately or severely reduced function) of left ventricular function (LVF) as noted by the echocardiographer for routinely performed postoperative echocardiography performed during routine follow-up.

    Measured: Within 30 days postoperatively.

  22. Urinary Oxygenation (Amsterdam UMC only)

    Mean urinary partial oxygen pressure (PuO2)

    Measured: From end to start of surgery and from transfer to ICU until discharge or 48 hours postoperatively.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Oct 2022
  2. Study start9 Jun 2023
  3. Primary completion14 May 2025
  4. Study completionSep 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
784 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05590143
Sponsor's protocol ID
MERCURI-2
Other IDs
2022-002453-25, 2024-515260-31-00, 10140022010003, NL81190.018.22, 2022.0795
Acronym
MERCURI-2
Status last verified
May 2025
First submitted
10 Oct 2022
Last updated
18 May 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Complete data collection methods and results will be shared with other researchers upon a formal request made to the principal investigator including a detailed motivation for the request.

Publications

  • Semler MW, Rice TW, Shaw AD, Siew ED, Self WH, Kumar AB, Byrne DW, Ehrenfeld JM, Wanderer JP. Identification of Major Adverse Kidney Events Within the Electronic Health Record. J Med Syst. 2016 Jul;40(7):167. doi: 10.1007/s10916-016-0528-z. Epub 2016 May 27.

    PubMed 27234478
  • Myles PS, Shulman MA, Heritier S, Wallace S, McIlroy DR, McCluskey S, Sillar I, Forbes A. Validation of days at home as an outcome measure after surgery: a prospective cohort study in Australia. BMJ Open. 2017 Aug 18;7(8):e015828. doi: 10.1136/bmjopen-2017-015828.

    PubMed 28821518
  • Federici S, Bracalenti M, Meloni F, Luciano JV. World Health Organization disability assessment schedule 2.0: An international systematic review. Disabil Rehabil. 2017 Nov;39(23):2347-2380. doi: 10.1080/09638288.2016.1223177. Epub 2016 Nov 7.

    PubMed 27820966
  • Stolk E, Ludwig K, Rand K, van Hout B, Ramos-Goni JM. Overview, Update, and Lessons Learned From the International EQ-5D-5L Valuation Work: Version 2 of the EQ-5D-5L Valuation Protocol. Value Health. 2019 Jan;22(1):23-30. doi: 10.1016/j.jval.2018.05.010. Epub 2019 Jan 2.

    PubMed 30661630
  • Lau D, Pannu N, James MT, Hemmelgarn BR, Kieser TM, Meyer SR, Klarenbach S. Costs and consequences of acute kidney injury after cardiac surgery: A cohort study. J Thorac Cardiovasc Surg. 2021 Sep;162(3):880-887. doi: 10.1016/j.jtcvs.2020.01.101. Epub 2020 Mar 3.

    PubMed 32299694
  • Menne J, Dumann E, Haller H, Schmidt BMW. Acute kidney injury and adverse renal events in patients receiving SGLT2-inhibitors: A systematic review and meta-analysis. PLoS Med. 2019 Dec 9;16(12):e1002983. doi: 10.1371/journal.pmed.1002983. eCollection 2019 Dec.

    PubMed 31815931
  • Gilbert RE, Thorpe KE. Acute kidney injury with sodium-glucose co-transporter-2 inhibitors: A meta-analysis of cardiovascular outcome trials. Diabetes Obes Metab. 2019 Aug;21(8):1996-2000. doi: 10.1111/dom.13754. Epub 2019 May 24.

    PubMed 31050116
  • Oosterom-Eijmael MJP, Hulst AH, de Oliveira NPM, Niesten ED, Wietsma NE, Gerritse BM, Scohy TV, Rettig TCD, Snellen FTF, Voogd MF, Godfried MB, de Boer RN, Wink J, van der Werff LMM, Cobbaert CM, Ruhaak LR, Eberl S, Preckel B, Hollmann MW, Schenk J, Hermanides J, van Raalte DH; MERCURI-2 Study Group. Dapagliflozin and Acute Kidney Injury Following Cardiac Surgery: A Randomized Clinical Trial. JAMA. 2026 Jul 30:e269268. doi: 10.1001/jama.2026.9268. Online ahead of print.

    PubMed 42530910
  • Oosterom-Eijmael M, Monteiro de Oliveira NP, Niesten ED, Tolsma M, Snellen FT, Gerritse BM, Scohy TV, Rettig T, Godfried MB, Voogd MF, Wink J, van der Werff LM, Eberl S, Preckel B, Hermanides J, van Raalte DH, Hulst AH; MERCURI-2 study group. Study protocol of the multicentre, randomised, triple-blind, placebo-controlled MERCURI-2 trial: promoting effective renoprotection in cardiac surgery patients by inhibition of sodium glucose cotransporter (SGLT)-2. BMJ Open. 2025 May 16;15(5):e095504. doi: 10.1136/bmjopen-2024-095504.

    PubMed 40379310
  • Snel LIP, Oosterom-Eijmael MJP, Rampanelli E, Lankadeva YR, Plummer MP, Preckel B, Hermanides J, van Raalte DH, Hulst AH. The effects of sodium-glucose transporter 2 inhibition on cardiac surgery-associated acute kidney injury: An open-label randomized pilot study. J Clin Anesth. 2025 Apr;103:111811. doi: 10.1016/j.jclinane.2025.111811. Epub 2025 Mar 27.

    PubMed 40153894

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Dapagliflozin 10 MG Oral Tablet [Farxiga] in people with Acute Kidney Injury and Cardiac Surgery, run by Amsterdam UMC at 6 sites in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 18 May 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 6 sites in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

AKI (time frame: Recorded daily until day 7 postoperatively or until discharge from hospital (earlier).). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05590143, which also lists 10 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 May 2025; AzTrials last refreshed its copy on 8 Nov 2026.

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