CompletedPhase 4ACTRN12623000248662

Route of administration of magnesium replacement in the ICU

Prospective, randomized, parallel group, electronic medical record (EMR)-embedded, clinical trial to determine whether the enteral route is non-inferior to parenteral magnesium replacement in critically ill patients with mild to moderate hypomagnesemia.


Sponsor

Royal Melbourne Hospital

Enrollment

330 participants

Start Date

Jun 7, 2023

Study Type

Interventional

Conditions

Summary

Magnesium is a crucial electrolyte and low serum magnesium concentrations must be treated promptly to avoid adverse effects. In the intensive care unit, critically ill patients are at risk of low magnesium concentrations magnesium ions are frequently administered via the enteral or parenteral (intravenous) route. There is sparse data as to which route to use but there is likely to be at least a tenfold cost differential between the enteral and parental preparations. In addition, there may be more waste and subsequent environmental impact associated with parenteral route. Given the potential but unproven advantages of the enteral route we wish to compare the safety and effectiveness of magnesium replacement via the enteral route and parenteral routes.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Inclusion Criteria1

  • All adult patients admitted to the RMH ICU who require magnesium replacement with serum magnesium level of <0.7 mmol/L

Exclusion Criteria4

  • Serum magnesium concentration <0.7 mmol/l and new cardiac arrhythmia; or serum magnesium concentration less than or equal to 0.35 mmol/l (ie., severe hypomagnesemia)
  • Either enteral or parenteral replacement is not possible (ie., no enteric feeding tube, intolerance of enteral feeding with gastric aspiration >300ml or no intravenous line)
  • Treating clinician believes that either enteral or parenteral magnesium is indicated for this patient
  • Patient's currently having enteral magnesium replacement order

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Interventions

This study will compare two routes of magnesium replacement in critically ill patients with hypomagnesemia; enteral or parenteral (intravenous). Both routes are current standard care. Those assigne

This study will compare two routes of magnesium replacement in critically ill patients with hypomagnesemia; enteral or parenteral (intravenous). Both routes are current standard care. Those assigned enteral route will receive either Mag-sup (magnesium aspartate dihydrate tablets) 500mg per tablet, which is equivalent to 37.4 mg or 1.55 mmol of elemental magnesium, or Blackmores BIO MAGNESIUM (magnesium-calcium-vit B6-vit D3) tablets (300mg of elemental magnesium or 12.5 mmol per tablet). The decision regarding single dose or regular (once, twice or three times per day) will be decided by the treating physician who will make their decision considering several factors including the severity of hypomagnesemia. Those assigned the parenteral route will receive magnesium sulfate, where the dose of magnesium will vary from 10 to 20 mmol and depend on decision by the ICU clinician. The magnesium sulfate is diluted in 100 ml of 0.9% saline and administered over a minimum of one hour. Medical records will be monitored frequently to ensure adherence to intervention arm.


Locations(1)

Royal Melbourne Hospital - City campus - Parkville

VIC, Australia

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