Major Depression Clinical Trials

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Examining the Effects of Escitalopram and Memantine on Pattern Separation in Major Depressive Disorder

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

This study seeks to examine the effects of treatment with a selective serotonin reuptake inhibitor (SSRI), escitalopram, a first-line treatment for depression, in combination with placebo or with extended-release memantine, on neuropsychological function, regional brain activity assessed by functional magnetic resonance imaging, and depressive symptoms, in participants with Major Depressive Disorder. Escitalopram is administered in an open-label fashion in this study; extended release memantine is administered in a double-blind, randomized, placebo-controlled manner.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 50
Healthy Volunteers: f
View:

• Age 18-50

• Current diagnosis of MDD without psychotic features assessed within three weeks of study enrollment

• 17-item Hamilton Depression Rating Scale score ≥17 assessed within 3 weeks of study enrollment

• Using an effective form of contraception at study enrollment and agrees to continue throughout study participation for individuals of child-bearing potential

• Capacity to provide informed consent

• Proficient in English

• Willing to provide emergency contact

Locations
United States
New York
New York State Psychiatric Institute (NYSPI)
RECRUITING
New York
Contact Information
Primary
Gabriella F Restifo-Bernstein, BA
gabriella.restifo@nyspi.columbia.edu
646-774-8138
Backup
Jeffrey M Miller, MD
jeffrey.miller@nyspi.columbia.edu
646-774-7613
Time Frame
Start Date: 2026-06-01
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 30
Treatments
Experimental: SSRI + Memantine
Placebo_comparator: SSRI + Placebo
Related Therapeutic Areas
Sponsors
Leads: Jeffrey Miller

This content was sourced from clinicaltrials.gov