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SODium BICarbonate for Metabolic Acidosis in the ICU

SODium BICarbonate for Metabolic Acidosis in the ICU

Not Recruiting
18 years and older
All
Phase 3

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Overview

This trial aims to assess if, among adults in the ICU with metabolic acidosis, an infusion of sodium bicarbonate diluted in 5% dextrose, compared with an infusion of 5% dextrose, reduces Major Adverse Kidney Events within 30 days of randomization.

Description

Background: Metabolic acidosis refers to any process that elevates the concentration of hydrogen ions in the body, and is commonly encountered in critical illness. Lactic acidosis, diabetic ketoacidosis, and hyperchloremic acidosis are major examples seen in the intensive care unit (ICU). Metabolic acidosis may impair cardiac function, and sodium bicarbonate can be used to normalise blood pH. Despite being in common clinical usage, the clinical efficacy of sodium bicarbonate is still uncertain. Previous studies exploring the effects of sodium bicarbonate therapy have been limited and of variable quality.

Aim: This trial aims to assess if, among adults in the ICU with metabolic acidosis, an infusion of sodium bicarbonate diluted in 5% dextrose, compared with an infusion of 5% dextrose, reduces Major Adverse Kidney Events within 30 days of randomization.

Study Design: Phase 3, international, multicentre, double-blind, randomised clinical trial.

Participants: Adult patients (≥ 18 years old), admitted to the ICU within 48 hours, receiving a continuous infusion of a vasopressor drug to maintain a mean arterial pressure > 65 mmHg (or a mean arterial pressure target set by the treating clinician), a dedicated line (central or peripheral) is available (or is about to be made available within 1 hour after randomisation), and within two hours prior to randomisation the participant has metabolic acidosis, defined as: 1) pH < 7.30; 2) BE ≤ -4 mEq/L; and 3) PaCO2 ≤ 45 mmHg.

Intervention: Patients will be randomly allocated in a 1:1 ratio to receive two treatments that are commonly used either an infusion of 5% dextrose (D5W) + sodium bicarbonate, or D5W alone, as a comparator. Study drug will be continuously infused targeting a pH 7.30 - 7.35 and a BE ≥ 0 mEq/L. The infusion will be maintained until this target is achieved and continued by titration thereafter for a maximum of 5 hours (to maintain target pH and base excess levels). All other aspects of care will be determined by the treating clinical team, including the use of additional fluid therapy, vasopressors, and other organ support modalities. Open-label sodium bicarbonate bolus infusion is allowed in both groups if clinically indicated.

Primary outcome: The primary outcome is the proportion of patients who meet one or more criteria for a major adverse kidney event within 30 days (MAKE 30). MAKE 30 is a composite of death, new receipt of renal-replacement therapy, or persistent renal dysfunction (defined as a final inpatient creatinine value ≥ 200% of the baseline value). All components of MAKE30 will be censored at hospital discharge or 30 days after enrollment, whichever comes first.

Eligibility

Inclusion Criteria:

        All the diagnostic criteria of metabolic acidosis below have to be fulfilled within the
        last 2 hours before randomisation (pH, PaCO2 and BE from the same blood gas), and a
        vasopressor is being infused continuously at the time of randomization.
          1. Adults (≥ 18 years);
          2. Receiving a continuous infusion of a vasopressor to maintain mean arterial pressure >
             65 mmHg (or a mean arterial pressure target set by the treating clinician);
          3. A dedicated intravenous line (central or peripheral) is available (or insertion of
             such a line is planned within the next hour); and
          4. Metabolic acidosis, defined as:
               1. pH < 7.30; and
               2. BE ≤ -4 mEq/L; and
               3. PaCO2 ≤ 45 mmHg for non-intubated patients or PaCO2 ≤ 50 mmHg for intubated
                  patients.
        Exclusion Criteria:
          1. Fulfilled all eligibility criteria greater than 48 hours ago; or
          2. Suspected clinically significant digestive or urinary tract loss of sodium bicarbonate
             (e.g., diarrhoea, ileostomy losses, renal tubular acidosis, or drainage of pancreatic
             or bile duct); or
          3. DKA; or
          4. Estimated glomerular filtration rate (eGFR) < 30 mL/min due to chronic kidney disease;
             or
          5. Currently receiving sodium bicarbonate at the moment of randomisation (doses of sodium
             bicarbonate prior to randomisation are allowed); or
          6. Currently receiving RRT (acute or chronic) or planned to start RRT in the next 3 hours
             (according to the treating clinical team); or
          7. Severe dysnatraemia (serum Na ≥ 155 mEq/L or < 120 mEq/L); or
          8. Hypokalaemia (serum K < 2.5 mEq/L); or
          9. Pulmonary oedema with PaO2 / FiO2 < 100; or
         10. Hypocalcaemia (iCa < 0.8mmol/L); or
         11. Patients admitted to the ICU after a drug overdose or intoxication (including alcohol
             intoxication); or
         12. Pregnancy or breastfeeding; or
         13. Death is deemed to be inevitable as a result of the current acute illness and either
             the treating clinician, the patient or the substitute decision maker are not committed
             to full active treatment; or
         14. Patients with a life expectancy < 30 days due to a chronic or underlying medical
             condition; or
         15. Considered to be at high risk of cerebral oedema by the treating clinician (e.g.
             traumatic brain injury or acute brain disease); or
         16. Clinician believes that being enrolled in intervention or control arm is not in the
             best interest of the patient; or
         17. Previous enrolment in this study.

Study details
    Metabolic Acidosis
    Shock

NCT05697770

Australian and New Zealand Intensive Care Research Centre

30 January 2026

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