Role of Magnesium Supplementation in the Treatment of Depression

Last updated: April 15, 2019
Sponsor: University of Vermont
Overall Status: Completed

Phase

2/3

Condition

Depression

Treatment

N/A

Clinical Study ID

NCT02466087
M15-337
  • Ages > 18
  • All Genders

Study Summary

The objective of this project is to test the hypothesis that magnesium supplementation will decrease depressive symptoms in adults.

This study takes place over 12 consecutive weeks. While the investigators will follow the volunteers for the full 12 weeks volunteers will only take magnesium supplements for 6 consecutive weeks. Volunteers will be randomly assigned to start the supplement at week 1 or week 7. Volunteers will take two supplement two times a day for a total of 248 mg elemental magnesium daily in the form of magnesium chloride. This amount of magnesium is less than the tolerable upper limit of 350 mg per day. The supplements will be provided. Volunteers will be asked to maintain their normal diet for the 12 weeks of the study.

The primary outcome measure is the PHQ-9 questionnaire, a validated measure of depression. Secondary measures include the GAD-7 for Anxiety and side effects.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • All adults at least 18 years of age

  • A Patient Health Questionnaire-9 (PHQ-9) score of greater or equal to 5 but less than 20

  • People who are currently being treated for depression are still eligible toparticipate but their treatment must be stable (no changes in medication dose or brandand/or no changes in therapy regimen for at least 2 months).

Exclusion

Exclusion Criteria:

  • Active delirium or dementia

  • Medicinal treatment for bipolar disorder, personality disorder or schizophrenia,

  • Glomerular Filtration Rate of less than 60

  • Irritable Bowel Disease

  • Inflammatory Bowel Disease

  • GERD

  • Gastritis

  • Pregnant as reported by potential volunteer

  • Myasthenia Gravis

  • Planned elective surgery

  • Currently taking

  • Long Term Antibiotics

  • Fluoroquinolone

  • Trientine or Penicillamine

  • Long Term Antivirals

  • Digoxin

  • Bisphosphonates

  • Eltrombopag

  • Opiods

  • Calcium Channel Blockers

  • Deferiprone

  • Doxercalciferol

  • Unable or unwilling to stop taking a magnesium supplement

Study Design

Total Participants: 126
Study Start date:
May 01, 2015
Estimated Completion Date:
December 31, 2016

Connect with a study center

  • University of Vermont

    Burlington, Vermont 05401
    United States

    Site Not Available

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