Phase 2
Completed N=10
Memantine Treatment of Compulsive Buying
Compulsive Buying
Source: ClinicalTrials.gov NCT00830375 ↗
Enrolled (actual)
10
Serious AEs
0.0%
Results posted
May 2012
Primary outcomePrimary: Yale Brown Obsessive Compulsive Scale Modified for CB (CB-YBOCS) — 22 units on a scale
Summary
This is an 8-week, open-labe study of memantine in the treatment of compulsive buying.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Yale Brown Obsessive Compulsive Scale Modified for CB (CB-YBOCS) |
22 | — |
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
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. Informational only — not medical advice.