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Efficacy of SGLT2 Inhibitors in Adults with Sepsis

Not Applicable
Recruiting
Conditions
Sepsis
SGLT2 Inhibitors
Organ Dysfunction Syndrome
Inflammation
Critically Ill
Interventions
Registration Number
NCT06473844
Lead Sponsor
Hospital Authority, Hong Kong
Brief Summary

Goal of this clinical trial is to examine the safety and efficacy of SGLT2 inhibitors on the clinical outcomes in patients with sepsis. Main study outcomes are as follows:

(i) Primary objective is to examine the efficacy and safety of SGLT2 inhibitors on clinical outcomes in patients with sepsis.

(ii) Secondary objective is to examine the effect of SGLT2 inhibitors on inflammatory markers in patients with sepsis.

Detailed Description

Sepsis is a leading epidemic in the world, affecting an estimated 48.9 million individuals annually. Patients who develop consequential organ failure requiring admission to the intensive care unit (ICU) has a mortality of up to 42%. In Hong Kong, sepsis was the second most common cause of ICU admission, accounting for 16.9% of the 14,068 patient admissions in 2018. Sepsis has remained as one of the top 10 leading causes of death in Hong Kong in the past decade.

Recent randomized controlled trials evaluating various therapies in sepsis have not yielded encouraging results. Targeted therapeutic options including adjunctive glucocorticoid therapy, intravenous vitamin C, and sepsis bundles have not been associated with improved clinical outcomes in patients with sepsis. Administration of antibiotics for source control has remained as the only treatment proven effective in sepsis for two decades. There is an urgent unmet need to identify therapies that may modulate the adverse outcomes of sepsis.

Sodium-glucose cotransporter-2 (SGLT2) inhibitors are a class of medication that reduces reabsorption of glucose from the kidneys by modulating the sodium-glucose cotransporter in the renal tubules. Although originally developed as a drug for type 2 diabetes, subsequent large randomized clinical trials have firmly established the clinical efficacy of SGLT2 inhibitors in improving cardiovascular and renal outcomes, irrespective of diabetes status. Patients who received SGLT2 inhibitors had a 32% relative risk reduction in all-cause mortality, 40% reduction in adverse renal outcomes, and 30% reduction in hospitalization for heart failure, compared with placebo.

The investigators hypothesize that SGLT2 inhibitors, as compared with placebo, will improve clinical outcomes of patients with sepsis who are receiving standard care.

(i) The primary objective is to examine the efficacy and safety of SGLT2 inhibitors on clinical outcomes in patients with sepsis.

(ii) The secondary objective is to examine the effect of SGLT2 inhibitors on inflammatory markers in patients with sepsis.

(iii) The tertiary objective is to examine the feasibility of conducting a multicenter double-blind randomized placebo-controlled trial in the ICUs of Hong Kong.

Adult patients (age≥18 years) with new onset sepsis and admitted to the ICU will be considered for recruitment based on the study inclusion/exclusion criteria. Eligible subjects will be randomly assigned to the intervention group or the control group in a 1:1 ratio. In the intervention group, the SGLT2 inhibitor empagliflozin 10mg orally daily will be given in addition to standard care until hospital discharge. In the control group, a placebo tablet once orally daily will be given in addition to standard care until hospital discharge. All patients will be followed up daily until hospital discharge or transfer to another facility. Blood samples will be collected and sent for an assay that measures the levels of key inflammatory markers.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Aged 18 years or above
  • New onset of sepsis within 48 hours defined according to the Sepsis-3 criteria. (≥2 SOFA)
  • Provision of signed and dated informed consent form from participant or surrogate
  • Ability to take and adhere to oral and enteral medication regimen
  • Willingness to comply
Exclusion Criteria
  • Current or recent use of SGLT2 inhibitors (within 12wks prior to randomization)
  • Impaired renal function
  • Clinically unstable or in refractory hypotension
  • History of ketoacidosis
  • Gastrointestinal surgery or GI absorption / malabsorption disorder
  • Pregnancy
  • Known allergic or hypersensitivity reactions to any SGLT2 inhibitors
  • Treatment with another investigational drug or other interventions within 30 days prior to trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SGLT2 inhibitor empagliflozinEmpagliflozin 10 MG10mg daily from recruitment to hospital discharge
PlaceboPlacebo1 tablet daily from recruitment to hospital discharge
Primary Outcome Measures
NameTimeMethod
Mortality28-day mortality

Patient 28-day mortality

Change in Sequential Organ Failure Assessment (SOFA) scoreBaseline and day 7 score

Score is based on lab results and clinical data. Higher SOFA scores indicate higher risk of ICU mortality. Lower SOFA scores predicts lower risk of ICU mortality.

Secondary Outcome Measures
NameTimeMethod
Interleukin-6, Interleukin-1 beta, TNF-a, IFN-gamma, Procalcitonin, C-reactive proteinBaseline and day 7

These markers are selected based on observed associations with SGLT2 inhibitors in experimental studies.

Trial Locations

Locations (3)

4/F Main Clinical Block and Trauma Centre, Prince of Wales Hospital, Shatin, New Territories, Hong Kong

🇭🇰

Hong Kong, Hong Kong

Adult Intensive Care Unit, Queen Mary Hospital, 102 Pok Fu Lam Road, Hong Kong

🇭🇰

Hong Kong, Hong Kong

The University of Hong Kong

🇭🇰

Hong Kong, Hong Kong

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