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Clinical Trial 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.


Clinical Trial 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


Related Conditions & MeSH terms


NCT number NCT00988663
Study type Interventional
Source University of Iowa
Contact
Status Withdrawn
Phase N/A
Start date November 2009
Completion date November 2009

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