Actively Recruiting

Phase 4
Age: 18Years - 90Years
All Genders
NCT03088852

Magnesium Deficiency In Patients Hospitalized in Internal Medicine Wards

Led by Frieda Wolf · Updated on 2025-03-18

330

Participants Needed

1

Research Sites

498 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Magnesium Deficiency In Patients Hospitalized in Internal Medicine Wards

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient is 18 years or older
  • Patient has hypomagnesemia with magnesium level 1.9 mg/dL or lower
  • Patient is admitted to internal medicine wards
  • Patient is able to give informed consent
Not Eligible

You will not qualify if you...

  • Patient unable to give consent
  • Patient admitted for an elective procedure
  • Patient in critical condition or dying
  • Advanced kidney disease with eGFR less than 15 ml/min or on dialysis
  • Severe diarrhea preventing use of magnesium citrate
  • Already receiving magnesium supplements
  • Severe malnutrition or life-threatening hypomagnesemia (serum level less than 1 mg/dL) requiring intravenous and oral magnesium replacement

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Emek Medical Center

Afula, Israel

Actively Recruiting

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Research Team

F

Frieda Wolf

CONTACT

R

Rotem Shvartzman

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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