Magnesium Sulfate Versus 5% Dextrose With Treatment Resistant Depression

This study is currently recruiting participants. (see Contacts and Locations)
Verified February 2014 by University of Miami
Sponsor:
Collaborator:
Life Extension Foundation Inc.
Information provided by (Responsible Party):
John E. Lewis, University of Miami
ClinicalTrials.gov Identifier:
NCT01597167
First received: May 9, 2012
Last updated: February 28, 2014
Last verified: February 2014
  Purpose

The proposed study is a 1-week, randomized, double-blind, placebo-controlled, trial to evaluate the efficacy of an IV infusion of magnesium sulfate on symptoms of treatment resistant mild and moderate depression in 20 males and females (21-70 years of age). Participants will be assessed at screening/baseline, day 1, day 2, day 7, and day 8. Each subject will be randomized in a double-blind fashion to receive either IV infusion of magnesium sulfate or 5% dextrose followed by a washout period of 5 days then crossover to receive either IV infusion of 5% dextrose or magnesium sulfate.


Condition Intervention
Depression
Dietary Supplement: Magnesium sulfate

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Double-blinded Randomized Study of IV Infusion of Magnesium Sulfate Versus 5% Dextrose in a Crossover Design in Male and Female Volunteers With Treatment Resistant Depression

Resource links provided by NLM:


Further study details as provided by University of Miami:

Primary Outcome Measures:
  • Magnesium levels in treatment resistant mild and moderate depression [ Time Frame: 8 days ] [ Designated as safety issue: No ]
    To investigate the magnesium deficient status in treatment-resistant mild and moderate depression patients via assay of 24-hour urine magnesium, blood magnesium, and EXATEST of intracellular magnesium of epithelial cells before and after IV infusion.

  • Self reported depression measures [ Time Frame: 8 days ] [ Designated as safety issue: No ]
    To assess the effectiveness of the magnesium sulfate infusion on the mean change in scores on the Hamilton Rating Scale for Depression and the Patient Health Questionnaire (PHQ-9) for depression.


Secondary Outcome Measures:
  • Correlation of magnesium levels with self reported measures of depression [ Time Frame: 8 days ] [ Designated as safety issue: No ]
    To correlate the levels of magnesium with the scores on the Hamilton Rating Scale for Depression and the Patient Health Questionnaire (PHQ-9) for depression


Estimated Enrollment: 20
Study Start Date: October 2011
Estimated Study Completion Date: September 2014
Estimated Primary Completion Date: September 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Magnesium sulfate crossover
IV infusion of magnesium sulfate followed by 5-day washout period and crossover to 5% dextrose (placebo)
Dietary Supplement: Magnesium sulfate
4 grams magnesium sulfate in 100 ml IV over 4 hours
Placebo Comparator: Placebo crossover
IV infusion of 5% dextrose with 5 day washout and crossover to magnesium sulfate
Dietary Supplement: Magnesium sulfate
4 grams magnesium sulfate in 100 ml IV over 4 hours

Detailed Description:

Purpose:

  1. To determine the magnesium deficient status in treatment-resistant mild and moderate depression patients via 24-hour urine magnesium assessment before and after IV magnesium infusion.
  2. Correlation of intracellular magnesium (EXATEST), urine magnesium, and serum magnesium as well as sensitivity to the IV magnesium infusion.
  3. To assess the effectiveness of magnesium sulfate infusion on treatment resistant mild and moderate depression patients.

Objectives:

Primary:

  1. To investigate the magnesium deficient status in treatment-resistant mild and moderate depression patients via assay of 24-hour urine magnesium, blood magnesium, and EXATEST of intracellular magnesium of epithelial cells before and after IV infusion.
  2. To assess the effectiveness of the magnesium sulfate infusion on the mean change in scores on the Hamilton Rating Scale for Depression and the Patient Health Questionnaire (PHQ-9) for depression.

Secondary:

1. To correlate the levels of magnesium with the scores on the Hamilton Rating Scale for Depression and the Patient Health Questionnaire (PHQ-9) for depression.

  Eligibility

Ages Eligible for Study:   21 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Potential participants must be English speaking.
  2. Between the ages of 21 and 70.
  3. Overall healthy and have no difficulty with digestion or absorption of food
  4. Have treatment-resistant depression defined as failure of clinical improvement after 6 weeks with an approved dose of a Selective Serotonin Uptake Inhibitor (SSRI), Serotonin-Norepinephrine Reuptake Inhibitor (SNRI), Selective Noradrenaline Reuptake Inhibitor (NRI), tricyclic antidepressant, or bupropion.
  5. Willing to provide informed consent to participate in the study.
  6. Willing and able to comply with all study procedures and data recording obligations for the entire length of the study.
  7. Able and willing to abstain from alcohol from 48 hours prior to the first intravenous infusion until after completion of the post-treatment follow-up visit (Day 2) and from 48 hours prior to the second intravenous infusion until after completion of the post-treatment follow-up visit (Day 8).
  8. If currently taking an SSRI for more than 90 days, have maintained the same dose for the past 90 days.
  9. A non-smoker or have quit smoking at least 6 months ago.

Exclusion Criteria:

  1. Currently enrolled (or have been in the last 30 days) in another research trial for investigative nutritional or other therapies thought to have an impact on depression.
  2. Currently taking a medication or nutritional supplement containing more than 100% RDA of magnesium (for women over age 31, it is 320 mg/day and for men over age 31, it is 420 mg/day) and unable to discontinue using it 14 days prior to the Day 1 visit. (Current use must be stopped 2 weeks before enrolling in the study and during trial.)
  3. Diagnosed with any medical condition, including diabetes, cardiovascular disease, pulmonary, renal, endocrine, hepatic, neurologic, psychiatric (except for depression), immunologic, hematologic, gastrointestinal, or metabolic disease requiring medical treatment that would preclude participation in the study.
  4. Taking Digoxin (used to treat congestive heart failure and to slow the heart rate in patients with atrial fibrillation.
  5. Taking penicillamine (also known as Cuprimine or Depen for Wilson's disease or rheumatoid arthritis).
  6. Taking any antibiotic (including tetracycline or a quinolone).
  7. Taking any psychotropic medication for any indication, except sedatives for sleep such as Zolpidem, in addition to the SSRI, SNRI, NRI, tricyclic antidepressant, or bupropion in the course of treatment for your depression.
  8. Taking a SSRI, SNRI, NRI, tricyclic antidepressant, or bupropion for less than 90 days or unable to maintain the same therapeutic regimen throughout the study duration.
  9. A history of any medical or surgical procedure that would preclude participation in the study.
  10. Diagnosed with gastrointestinal disorders that could lead to uncertain resorption of the study supplements.
  11. Pregnant, plan to become pregnant, or currently breast feeding.
  12. Unwilling to avoid pregnancy (use medically-acceptable birth control method during the study with at least one method for the period of one month prior to beginning of the study until at least three months after study completion or are surgically sterile or postmenopausal (at least 12 months without a period).
  13. Systolic blood pressure >160 mmHg or diastolic blood pressure >90 mmHg.
  14. Had any of the following abnormal laboratory test values: (a) bilirubin > 2x upper normal limit, (b) AST and ALT > 2x upper normal limit, (c) serum creatinine > 1.5 mg/dl, (d) blood glucose below 80 mg/dl or above 110 mg/dl, (e) calcium level < 8.6 mg/dl, or (f) triglycerides >200 mg/dl.
  15. Currently undergoing any chemotherapy or radiation treatment for cancer, have an active malignancy, or have had within the past 5 years any type of malignancy, other than non-melanomatous skin malignancies.
  16. A history of substance abuse (e.g., alcohol, opiates, benzodiazepines, or amphetamines).
  17. Currently consume more than 6 standard alcoholic drinks a week (A standard alcoholic drink is defined as one bottle/can of beer, one glass of wine, or one ounce of hard liquor.).
  18. Diagnosed with a terminal illness.
  19. Donated blood in the last 30 days.
  20. Any severe, acute illness within the last five days.
  21. Have a pacemaker or internal medical device.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01597167

Contacts
Contact: Steven Atlas 305-243-9373 SAtlas@med.miami.edu
Contact: Johanna Lopez 305-243-9373

Locations
United States, Florida
University of Miami Clinical Research Building Recruiting
Miami, Florida, United States, 33136
Sponsors and Collaborators
University of Miami
Life Extension Foundation Inc.
Investigators
Principal Investigator: John Lewis, PhD University of Miami
  More Information

No publications provided

Responsible Party: John E. Lewis, Associate Professor of Psychiatry and Behavioral Sciences, University of Miami
ClinicalTrials.gov Identifier: NCT01597167     History of Changes
Other Study ID Numbers: 20110168
Study First Received: May 9, 2012
Last Updated: February 28, 2014
Health Authority: United States: Institutional Review Board

Keywords provided by University of Miami:
mild moderate treatment-resistant depression
magnesium sulfate

Additional relevant MeSH terms:
Depression
Depressive Disorder
Behavioral Symptoms
Mood Disorders
Mental Disorders
Magnesium Sulfate
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Pharmacologic Actions
Central Nervous System Agents
Therapeutic Uses
Anesthetics
Central Nervous System Depressants
Anti-Arrhythmia Agents
Cardiovascular Agents
Anticonvulsants
Calcium Channel Blockers
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Tocolytic Agents
Reproductive Control Agents

ClinicalTrials.gov processed this record on July 24, 2014