Dextromethorphan-Bupropion versus SSRIs for Major Depressive Disorder
Dextromethorphan-Bupropion
+ SSRIs
Mental Disorders+1
+ Depressive Disorder, Major
+ Depressive Disorder
Treatment Study
Summary
Study start date: May 6, 2025
Actual date on which the first participant was enrolled.This study investigates the effectiveness of a combination of two drugs, dextromethorphan and bupropion, compared to commonly used medications known as SSRIs, like sertraline or escitalopram, in treating major depressive disorder. The focus is on adult patients who are experiencing symptoms of major depression. By comparing these treatments, the study aims to determine if the new drug combination can potentially offer better relief from depression symptoms than the standard SSRI treatments. Understanding the effectiveness of these options is crucial as it might provide new insights and improvements in managing major depression. Participants in this study are divided into two groups, with one group receiving the dextromethorphan-bupropion combination and the other group receiving an SSRI treatment. The treatment period lasts for six weeks. Researchers will measure how well the participants respond to the treatments by using a depression rating scale to track remission rates. Additionally, they will examine changes in the severity of depressive symptoms and monitor any side effects or issues with tolerability, ensuring the safety of the treatments.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.80 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 60 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
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 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 Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 2 locations
Department of Psychiatry, Combined Military Hospital Nowshera
Nowshera, Pakistan