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Comparison of two methods of administering magnesium through continuous infusion (?? hours) and short-term infusion (? hours) in the correction of hypomagnesemia

Comparison of two methods of administering magnesium through continuous infusion (?? hours) and short-term infusion (? hours) in the correction of hypomagnesemia in patients admitted to the ICU of Sina Hospital: a clinical pilot study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200322046833N4
Enrollment
30
Registered
2024-01-05
Start date
2024-01-21
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hypomagnesemia. Disorders of magnesium metabolism

Interventions

Intervention 1: Intervention group: Correction of the patient s hypomagnesemia by administering continuous infusion of magnesium sulfate (7.5 gram magnesium sulfate manufactured by Daro Pakhsh industr

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Hypomagnesemia patients hospitalized in the intensive care unit Less than 96 hours have passed since ICU admission. written consent to enter the study

Exclusion criteria

Exclusion criteria: Magnesium serum concentration higher than 4 mg/dl Stage IV, V CKD based on the Cockcroft-Gault formula heart rate less than 50 times per minute, 2nd and 3rd degree heart block receiving a high dose of furosemide (more than 3 mg/hr) The need to receive magnesium outside the protocol History of muscle weakness disease (MS, Guillain-Barre, botulism, myasthenia gravis) Refractory shock (EP ? NEP > ?? mcg/min ) survival less than 48 hours Patients with AKI massive blood transfusion unable to take a urine sample for any reason?

Design outcomes

Primary

MeasureTime frame
The number of patients who have more than 50% magnesium retention at the end of the study. Timepoint: Urine collection 24 hours after magnesium administration. Method of measurement: 24-hour urine collection and examination of magnesium excreted in 24-hour urine.

Secondary

MeasureTime frame
Change in the percentage of urinary magnesium excreted compared to the baseline condition. Timepoint: Measurement of urine magnesium before starting treatment and after finishing treatment. Method of measurement: Measurement of urine magnesium after 24hour.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarhad Najmeddin

Tehran University of Medical Sciences

f-najmeddin@sina.tums.ac.ir+98 21 6695 4709

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026