Magnesium Sulfate Versus 5% Dextrose With Treatment Resistant Depression

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.

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.