Efficacy of Dextromethorphan-Bupropion Versus SSRIs in the Treatment of Major Depressive Disorder

Last updated: May 3, 2026
Sponsor: Asad Ullah Jan
Overall Status: Completed

Phase

N/A

Condition

Depression

Treatment

Dextromethorphan-Bupropion

SSRIs

Clinical Study ID

NCT06957223
CMHNSR-REF-16
  • Ages 18-60
  • All Genders

Study Summary

The study aims to compare the antidepressant effects of a dextromethorphan-bupropion combination versus standard SSRI therapy in adult patients with major depressive disorder. Participants will be randomized into two groups: one receiving dextromethorphan-bupropion and the other receiving an SSRI (e.g., sertraline or escitalopram). Treatment will last for 6 weeks, with assessments at baseline and study completion. The primary outcome will be the remission rate measured by a validated depression rating scale. Secondary outcomes include change in depressive symptoms severity and safety/tolerability measures.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Diagnosed with major depressive disorder (MDD) per DSM-5 criteria.

Baseline depression score indicating moderate to severe depression

Ability to provide informed consent

Willing to comply with study requirements

Exclusion

Exclusion Criteria:

History of bipolar disorder, schizophrenia, or other psychotic disorders

Current substance use disorder (within past 6 months)

Active suicidal ideation requiring urgent intervention

Pregnancy or breastfeeding

Known hypersensitivity to study medications

Study Design

Total Participants: 80
Treatment Group(s): 2
Primary Treatment: Dextromethorphan-Bupropion
Phase:
Study Start date:
May 06, 2025
Estimated Completion Date:
December 31, 2025

Connect with a study center

  • Combined Military Hospital

    Nowshera, KPK 25770
    Pakistan

    Site Not Available

  • Department of Psychiatry, Combined Military Hospital Nowshera

    Nowshera, KPK 25770
    Pakistan

    Site Not Available

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