MedPath

NMDA Modulation in Major Depressive Disorder in Late- Life

Phase 2
Completed
Conditions
Depressive Disorder, Major
Interventions
Drug: Placebo - Cap
Registration Number
NCT03414931
Lead Sponsor
Chang Gung Memorial Hospital
Brief Summary

Major depressive disorder (MDD) is a complex and multi-factorial disorder. Most of the current antidepressants are based upon the monoamine hypothesis which cannot fully explain the etiology of depression. Many elderly patients have significant side effects after treatment with antidepressants which hamper the motivation for treatment and medication adherence. NMDA hypofunction has been implicated in the pathophysiology of depression. MDD in the elderly is often associated with cognitive deficits which are not necessarily recovered by current antidepressants. The NMDA receptor regulates synaptic plasticity, memory, and cognition. In our previous studies, cognitive improvement has been observed with treatment of NMDA enhancers. Therefore, this study will examine the efficacy and safety as well as cognitive function improvement of NMDAE in the treatment of MDD in the elderly by comparing with sertraline (a selective serotonin reuptake inhibitor \[SSRI\]) and placebo.

The investigator will enroll elderly patients with MDD for an 8-week treatment. All patients will be randomly assigned into three groups: NMDAE, sertraline, or placebo. The investigator will biweekly measure clinical performances. Cognitive functions will be assessed at baseline and at endpoint of treatment by a battery of tests. The investigator hypothesize that NMDAE can safely yield better efficacy than placebo and sertraline for elderly patients with MDD.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
136
Inclusion Criteria
  • Have a DSM-IV (American Psychiatric Association 1994) diagnosis of MDD
  • 17-item Hamilton Rating Scale for Depression total score ≥ 18
  • Free of psychotropic drugs for at least 2 weeks
  • Have a Mini-Mental State Examination (Folstein, Folstein et al. 1975) score ≥ 20
Exclusion Criteria
  • Current substance abuse or history of substance dependence in the past 6 months
  • Use of depot antipsychotics in the past 6 months
  • History of epilepsy, head trauma, stroke or other serious medical or neurological illness
  • Bipolar depression, schizophrenia or other psychotic disorder
  • Moderate-severe suicidal risks
  • Severe cognitive impairment
  • Initiating or stopping formal psychotherapy within six weeks prior to enrollment
  • A history of poor response to SSRIs or other antidepressants
  • A history of previously received electroconvulsive therapy
  • A history of severe adverse reaction to SSRIs or other antidepressants
  • Inability to follow protocol

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
NMDAENMDAAn NMDA enhancer
SSRISertralineSertraline
PlaceboPlacebo - CapPlacebo
Primary Outcome Measures
NameTimeMethod
Change from baseline of 17-item Hamilton Rating Scale for DepressionWeek 0, 2, 4, 6, 8

Assessment of depressive symptoms. The 17-item Hamilton Rating Scale for Depression will be measured biweekly.

Change from baseline of Perceived Stress ScaleWeek 0, 2, 4, 6, 8

Assessment of stress and anxiety symptoms. The Perceived Stress Scale will be measured biweekly

Secondary Outcome Measures
NameTimeMethod
Change from baseline of Beck's Suicide ScaleWeek 0, 2, 4, 6, 8

Assessment of suicidal symptoms. The Beck's Suicide Scale will be measured biweekly

Drop out rateWeek 0, 2, 4, 6, 8

The rate of drop out

Change from baseline of Geriatric Depression ScaleWeek 0, 2, 4, 6, 8

Assessment of geriatric depressive symptoms. The Geriatric Depression Scale will be measured biweekly

Cognitive functionWeek 0, 8

A battery of tests to assess the cognitive function including speed of processing (category fluency) and verbal and nonverbal working memory

Clinical Global ImpressionWeek 2, 4, 6, 8

Assessment of global improvement

Trial Locations

Locations (2)

China Medical University Hospital

🇨🇳

Taichung, Taiwan

Chang Gung Memorial Hospital

🇨🇳

Kaohsiung, Taiwan

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