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Phase 2 N=12 Treatment

Memantine in the Treatment of Kleptomania

Kleptomania

Enrolled (actual)
12
Serious AEs
0.0%
Results posted
Mar 2014
Primary outcome: Primary: Yale Brown Obsessive Compulsive Scale Modified for Kleptomania (KM-YBOCS) — 5.4 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Memantine (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Chicago
Primary completion
May 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Yale Brown Obsessive Compulsive Scale Modified for Kleptomania (KM-YBOCS)
5.4
SECONDARY
Kleptomania Symptom Assessment Scale (K-SAS)
12.3
SECONDARY
Clinical Global Impression Severity Scales (CGI)
2.2

Summary

The goal of the proposed study is to evaluate the efficacy and safety of memantine in kleptomania.

Eligibility Criteria

Inclusion Criteria

  • men and women age 18-65
  • current KM using the clinician-administered Structured Clinical Interview for Kleptomania (SCI-K)
  • stealing behavior within 2 weeks prior to enrollment.

Exclusion Criteria

  • infrequent stealing (i.e. less than one time per week) that does not meet proposed criteria for kleptomania (KM)
  • unstable medical illness or clinically significant abnormalities on laboratory tests or physical examination at screen
  • history of seizures
  • myocardial infarction within 6 months
  • current pregnancy or lactation, or inadequate contraception in women of childbearing potential
  • a need for medication other than memantine with possible psychotropic effects or unfavorable interactions
  • clinically significant suicidality
  • current Axis I disorder determined by the Structured Clinical Interview for the DSM (SCID) and SCID-compatible modules for impulse control disorders (Grant et al., 2005), except for nicotine dependence
  • lifetime history of bipolar disorder type I or II, dementia, schizophrenia, or any psychotic disorder determined by SCID
  • current or recent (past 3 months) DSM-IV substance abuse or dependence
  • positive urine drug screen at screening
  • initiation of psychotherapy or behavior therapy within 3 months prior to study baseline
  • previous treatment with memantine; and 14) treatment with investigational medication or depot neuroleptics within 3 months, with fluoxetine within 6 weeks, or with other psychotropics within 2 weeks prior to study baseline.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00880685). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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