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Clinical Trials/NCT00988663
NCT00988663WithdrawnNot Applicable

Memantine Augmentation of Electroconvulsive Therapy in Patients With Major Depression

Jerrry L Lewis1 site in 1 countryStarted: November 2009Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Sponsor
Locations
1
Primary Endpoint
Assessment of whether Memantine protects memory and cognitive impairment caused by ECT.

Study Overview

Brief Summary

The purpose of this study is to determine whether memantine will enhance the therapeutic of effect on depression and prevent memory and other cognitive problems caused by ECT.

Detailed Description

Patients will be assigned randomly either to a treatment group or a placebo groups. All patients in both groups will be receiving standard ECT. The treatment group will receive memantine. All patients will be given a battery of cognitive tests and test of depression before ECT treatments start, after the 6th ECT treatment and after the completions of ECT. An analysis will be performed to see if memantine causes any impact on the response to ECT and prevents memory and cognitive impairment.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Meets criteria for Major Depressive disorder

Exclusion Criteria

  • Neurological disease
  • Mental retardation
  • Seizure disorder

Arms & Interventions

Memantine arm

Active Comparator

Patient receiving ECT and Memantine

Intervention: memantine (Drug)

placebo

Placebo Comparator

25 patients receiving ECT will will receive placebo

Intervention: memantine (Drug)

placebo

Placebo Comparator

25 patients receiving ECT will will receive placebo

Intervention: Placebo (Drug)

Outcomes

Primary Outcomes

Assessment of whether Memantine protects memory and cognitive impairment caused by ECT.

Time Frame: 6 to 8 weeks

Secondary Outcomes

  • Whether memantine will improve response of Depression to Electroconvulsive therapy.(6-8 weeks)

Investigators

Sponsor
Jerrry L Lewis
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Jerrry L Lewis

Principal Investigator

University of Iowa

Study Sites (1)

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