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The Impact of Memantine on Electroconvulsive Therapy (ECT): Will it Improve Response and Protect Against Cognitive Problems?

Not Applicable
Withdrawn
Conditions
Major Depressive Disorder
Interventions
Drug: Placebo
Registration Number
NCT00988663
Lead Sponsor
Jerrry L Lewis
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.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Meets criteria for Major Depressive disorder
Exclusion Criteria
  • Neurological disease
  • Mental retardation
  • Seizure disorder

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
placeboPlacebo25 patients receiving ECT will will receive placebo
Memantine armmemantinePatient receiving ECT and Memantine
placebomemantine25 patients receiving ECT will will receive placebo
Primary Outcome Measures
NameTimeMethod
Assessment of whether Memantine protects memory and cognitive impairment caused by ECT.6 to 8 weeks
Secondary Outcome Measures
NameTimeMethod
Whether memantine will improve response of Depression to Electroconvulsive therapy.6-8 weeks

Trial Locations

Locations (1)

University of Iowa hosptitals and clinic

🇺🇸

Iowa City, Iowa, United States

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