Magnesium Bisglycinate in Major Depressive Disorder

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAll India Institute of Medical Sciences, Bhubaneswar

About this trial

Depression is a common illness that can affect a person's mood, sleep, energy, ability to work, and overall quality of life. While medicines are available to treat depression, many people do not get complete relief from their symptoms. This study will evaluate whether adding a magnesium supplement in the form of magnesium bisglycinate to regular antidepressant treatment can help improve symptoms of depression. Adults with depression who are already receiving treatment will be randomly assigned to receive either magnesium bisglycinate or a placebo (an inactive substance) along with their usual medication. The study will compare the two groups to see whether the supplement leads to greater improvement in symptoms, sleep, and day-to-day functioning. Information on any side effects will also be collected. The findings may help determine whether magnesium bisglycinate can be used as a safe and affordable additional treatment for people with depression.

Eligibility criteria

Qualifiers

Patients with a diagnosis of Major Depressive Disorder (MDD) as per DSM-5 criteria.

Patients of either sex within the age group of 18-65 years.

Mild to severe depression, defined as a baseline MADRS score ≥7.

Currently receiving a stable dose of antidepressant monotherapy (SSRI or SNRI) in equivalent doses.

Disqualifiers

Known hypersensitivity or allergy to magnesium supplements or glycine.

History of renal impairment (previous history of AKI, CKD, currently on dialysis).

Diagnosis of bipolar affective disorder, schizoaffective disorder, schizophrenia, or any other psychotic disorder.

Active suicidal ideation with intent or a recent suicide attempt (within the past 6 months), as assessed by the treating psychiatrist.

Trial design

Treatments tested in this trial

  • Magnesium Bisglycinate
  • Microcrystalline cellulose

Treatment groups

84 Participants
are divided into 2 treatment groups