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NCT03088852

Magnesium Deficiency In Patients Hospitalized in Internal Medicine Wards

Recruiting now Phase 4 Last updated 16 March 2025
What this trial tests

Phase 4 trial testing Magnesium Citrate 100 MG in Hypomagnesemia in 330 participants. Currently enrolling.

Timeline
10 May 2017
Primary endpoint
1 December 2025
1 December 2026

Quick facts

Lead sponsorFrieda Wolf
PhasePhase 4
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment330
Start date10 May 2017
Primary completion1 December 2025
Estimated completion1 December 2026
Sites1 location across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Frieda Wolf — full company profile →

Who can join

Adults 18 to 90, any sex, with Hypomagnesemia. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hypomagnesemia

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03088852.