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Magnesium Deficiency In Patients Hospitalized in Internal Medicine Wards

Magnesium Deficiency In Patients Hospitalized in Internal Medicine Wards

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03088852
Enrollment
330
Registered
2017-03-23
Start date
2017-05-10
Completion date
2026-12-31
Last updated
2025-03-18

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

Conditions

Hypomagnesemia

Brief summary

Hypomagnesemia is a common entity in the inpatient and outpatient setting. in previous retrospective study hypomagnesemic patients have higher mortality and longer hospitalization. whether hypomagnesemia is merely a marker of poor prognosis, or whether replacing it can improve outcomes is unclear. The current standard of care is to discharge these patients without workup or further treatment, even if patients had received intravenous therapy while hospitalized. The investigator wish to examine prospectively whether giving replacement therapy affects mortality, length of hospital stay and overall well-being. In order to replete intracellular levels and replete magnesium stores, magnesium should be given for several months.

Interventions

DRUGMagnesium Citrate 100 MG

initial intravenous treatment: Patients with magnesium levels 1-1.5 mg/dL will receive 2-4 grams of magnesium sulfate in the first 24 hours. Patients with magnesium levels 1.6-1.9 mg/dL will receive 1 gram of magnesium sulfate. participants with magnesium level ≥1 mg/dL, will be randomized, and oral magnesium therapy, Magnesium Citrate, ( or no treatment) will be started, and continued for at least three months. The experimental group will receive 400mg magnesium daily in two divided doses.

Sponsors

Frieda Wolf
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Any patient admitted over the age of 18, has hypomagnesemia (magnesium level ≤1.9 mg/dL) and is able to give consent.

Exclusion criteria

* A patient unable to give consent. * A patient admitted for an elective procedure. * A patient in critical condition or dying. * Patients with advanced kidney disease with eGFR\<15ml/min or on dialysis. * Patients with severe diarrhea, precluding use of magnesium citrate. * Patients already receiving magnesium supplements. * Patients with severe malnutrition or life-threatening hypomagnesemia (serum level \<1mg/dL), requiring intravenous and oral replacement of magnesium.

Design outcomes

Primary

MeasureTime frameDescription
compare mortalityone yearTo compare mortality between the population receiving magnesium and the population receiving standard care: ie no replacement.

Secondary

MeasureTime frameDescription
Hospitalizationone yearLength in days of hospitalization.

Other

MeasureTime frameDescription
causes for hypomagnesemiaone yearThe investigators will attempt to ascertain the causes for hypomagnesemia from the data collected (medications, diarrhea, malnutrition, etc)
re-hospitalizationone yearre-hospitalization for any cause
Subjective well-beingone yearsymptoms and overall well-being of the patients: a questionaire will be administered at the beginning of the study and at each visit regarding subjective feelings of well being, symptoms of pain, cramping and diarrhea, and overall functional capacity

Countries

Israel

Contacts

Primary ContactFrieda Wolf
friedawo@clalit.org.il972-4-6495476
Backup ContactRotem Shvartzman
rotem_sw@clait.org.il972-4-6495351

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026