Effect of Protocolized Magnesium Replacement on Mortality and Atrial Fibrillation in Critically Ill Patients
Sponsor: Scarborough General Hospital • ClinicalTrials.gov ID: NCT07173855
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In patients with critical illness, such as severe infections, heart attacks, or respiratory failure, most intensive care units (ICUs) measure magnesium levels and give supplemental doses of magnesium when levels are below certain targets. However, the best targets are unknown. The goal of this clinical trial is to study protocols for magnesium supplementation in people with critical illness, comparing a protocol with higher target level to a protocol with a lower target level. The main question this study aims to answer is whether magnesium supplementation protocols targeting a higher or lower level lead to better 30-day survival and less atrial fibrillation. Participants will not have to do any specific tasks, undergo any additional tests, or complete any surveys.
Interventions
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Magnesium sulfate administration
(Drug)
Magnesium sulfate is used in both arms for magnesium replacement.
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Magnesium oxide
(Drug)
In the higher-target arm, magnesium oxide 420mg po q12h x 2 is one of the options available for magnesium replacement when magnesium levels lie between 0.75 and 0.95mmol/L.
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Magnesium glucoheptonate
(Drug)
Magnesium glucoheptonate 30mL po q12h x 2 is an oral option for magnesium replacement in the higher-target arm.
Eligibility criteria
Conditions
Locations
- Lakeridge Health Ajax-Pickering — Ajax, Ontario, Canada
- Lakeridge Health Bowmanville — Bowmanville, Ontario, Canada
- Lakeridge Health Oshawa — Oshawa, Ontario, Canada
- Scarborough Centenary Hospital — Toronto, Ontario, Canada
- Scarborough General Hospital — Toronto, Ontario, Canada
- Scarborough Birchmount Hospital — Toronto, Ontario, Canada
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Learn MoreOfficial Source
Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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