Could a common mineral boost antidepressants? new trial investigates
NCT ID NCT07458022
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This phase 2 trial tests whether adding magnesium to a standard SSRI antidepressant works better than the SSRI alone for adults with major depressive disorder. Fifty participants will be randomly assigned to receive either the combination or just the SSRI. The main goal is to see if depression scores improve more with the added magnesium after 4 weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- magnesium
- What this could lead to
- If it works, this could point toward a simple, low-cost way to boost the effectiveness of standard antidepressants for people with major depression.
- What could go wrong
- This is a small, early-phase trial with only 50 participants, so results may not apply to everyone. It's also not yet clear if adding magnesium is safe or effective long-term.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
50 people
The number who actually took part.
- Started
-
Dec 2025
- Expected to finish
-
Apr 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: All patients of above 18 years diagnosed with DSM who had MDD and receiving SSRI alone and SSRI plus magnesium. Exclusion Criteria: Individuals who recently underwent treatment with electroconvulsive therapy, have a history of epilepsy or other severe neurological problems, have experienced a head injury, are cognitively impaired, and have comorbid conditions such as liver, renal, cardiovascular, neurological, or endocrine, or respiratory problems, or are pregnant or nursing mothers
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Combined Military Hospital (CMH)
Multan, Punjab Province, 60000, Pakistan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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