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Phase 2 N=10 Treatment

Memantine Treatment of Compulsive Buying

Compulsive Buying

Enrolled (actual)
10
Serious AEs
0.0%
Results posted
May 2012
Primary outcome: Primary: Yale Brown Obsessive Compulsive Scale Modified for CB (CB-YBOCS) — 22 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 Minnesota
Primary completion
Aug 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Yale Brown Obsessive Compulsive Scale Modified for CB (CB-YBOCS)
22

Summary

This is an 8-week, open-labe study of memantine in the treatment of compulsive buying.

Eligibility Criteria

Inclusion Criteria

  • men and women age 18-65
  • current CB using the clinician-administered Structured Clinical Interview for Compulsive buying (SCI-CB)
  • buying behavior within 2 weeks prior to enrollment

Exclusion Criteria

  • infrequent buying (i.e. less than one time per week) that does not meet proposed criteria for CB
  • 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 SCID and SCID-compatible modules for impulse control disorders, 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
  • 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 (NCT00830375). 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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