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OpenTrials
Completed

NCT Number: NCT00830375

Memantine Treatment of Compulsive Buying

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

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Ambulatory Research Center, Minneapolis, Minnesota, United States

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About this study

The goal of the proposed study is to evaluate the efficacy of memantine in the treatment of compulsive buying. Sixteen subjects meeting criteria for compulsive buying will receive 8 weeks of open-label memantine. The hypothesis to be tested is that memantine will be effective and well tolerated in patients with compulsive buying. The proposed study will provide needed data on the treatment of a disabling disorder that currently lacks a clearly effective treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Memantine

Drug

10-30mg, by mouth, daily

Other names: Namenda

Primary outcomes

  1. Yale Brown Obsessive Compulsive Scale Modified for CB (CB-YBOCS)

    Time frame: from study start to study end (8-weeks) and is Investigator rated

    The CB-YBOCS is a reliable and valid, 10-item, clinician-administered scale that rates buying symptoms within the last seven days, on a severity scale from 0 to 4 for each item (total scores range from 0 to 40 with higher scores reflecting greater illness severity). Scores ranging from 0 to 10 reflect minimal or mild symptoms; scores from 11 to 20 suggest moderate symptoms; severe symptoms are associated with scores from 21 to 30; and scores greater than 30 reflect extreme buying symptoms

Sponsors and collaborators

Lead sponsor

University of Minnesota

Other

Registry information

Official study title

Memantine Treatment of Compulsive Buying: An Open-Label Study

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Jan 27, 2009
Registry last updated
Jul 29, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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