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Selective Serotonin Reuptake Inhibitor

Escitalopram for Depression

Phase 4
Waitlist Available
Led By Christine DeLorenzo, PhD
Research Sponsored by Stony Brook University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8 weeks
Awards & highlights

Summary

Despite current medications, morbidity and mortality of Major Depressive Disorder (MDD) remain high. According to the World Health Organization, MDD affects 121 million people worldwide, and is projected to be the second leading cause of global disability by 2020. Monotherapy with selective serotonin reuptake inhibitors (SSRIs) is the most widely used treatment for MDD. However, on average, SSRIs require six weeks for onset of action, and two-thirds of those on SSRIs fail to achieve remission. Compounding this problem, patients with residual symptoms are significantly more likely to discontinue treatment or relapse, be hospitalized for medical and psychiatric conditions, or die of suicide and other causes. Although eliminating ineffective treatment trials would significantly reduce patient suffering and healthcare costs,clinicians currently do not have the tools to objectively select treatment based on an individual's likelihood of remission. Therefore, there is an urgent need to identify markers predictive of an individual's SSRI treatment outcome. Developing this personalized treatment requires increased understanding of the relationship between pretreatment neurobiology, SSRI-induced biological changes, and the corresponding symptom improvements.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change From Baseline in Hamilton Depression Rating Scale at 8 Weeks
Secondary study objectives
Bias of VersaPET Scanner From Measurements Taken at the Wrist and Ankle
Change From Baseline in Metabolic Rate of Glucose (MRGlu), Quantified Using Arterial Blood Analysis, at 8 Weeks
Correlation Coefficient of VersaPET Scanner From Measurements Taken at the Wrist or Ankle
+1 more

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: EscitalopramActive Control1 Intervention
Active Comparator: Escitalopram (Lexapro) 10mg Week 1, 20mg Weeks 2 and 3, and 30mg for Weeks 4 to 8 (or until 12 for patients close to remission)
Group II: PlaceboPlacebo Group1 Intervention
Lactose pill manufactured to mimic Escitalopram pill

Find a Location

Who is running the clinical trial?

Stony Brook UniversityLead Sponsor
222 Previous Clinical Trials
41,843 Total Patients Enrolled
16 Trials studying Depression
7,400 Patients Enrolled for Depression
Christine DeLorenzo, PhDPrincipal InvestigatorStony Brook University
1 Previous Clinical Trials
42 Total Patients Enrolled
1 Trials studying Depression
42 Patients Enrolled for Depression
~8 spots leftby Sep 2025