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Memantine Treatment of Compulsive Buying

Memantine Treatment of Compulsive Buying: An Open-Label Study

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00830375
Enrollment
10
Registered
2009-01-27
Start date
2008-12-01
Completion date
2010-08-01
Last updated
2019-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Compulsive Buying

Keywords

Buying, Shopping, Impulse Control

Brief summary

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

Detailed description

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.

Interventions

DRUGMemantine

10-30mg, by mouth, daily

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. men and women age 18-65 2. current CB using the clinician-administered Structured Clinical Interview for Compulsive buying (SCI-CB) 3. buying behavior within 2 weeks prior to enrollment

Exclusion criteria

1. infrequent buying (i.e. less than one time per week) that does not meet proposed criteria for CB 2. unstable medical illness or clinically significant abnormalities on laboratory tests or physical examination at screen 3. history of seizures 4. myocardial infarction within 6 months 5. current pregnancy or lactation, or inadequate contraception in women of childbearing potential 6. a need for medication other than memantine with possible psychotropic effects or unfavorable interactions; 7. clinically significant suicidality; 8. current Axis I disorder determined by the SCID and SCID-compatible modules for impulse control disorders, except for nicotine dependence 9. lifetime history of bipolar disorder type I or II, dementia, schizophrenia, or any psychotic disorder determined by SCID 10. current or recent (past 3 months) DSM-IV substance abuse or dependence; 11. positive urine drug screen at screening 12. initiation of psychotherapy or behavior therapy within 3 months prior to study baseline 13. previous treatment with memantine 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

Design outcomes

Primary

MeasureTime frameDescription
Yale Brown Obsessive Compulsive Scale Modified for CB (CB-YBOCS)from study start to study end (8-weeks) and is Investigator ratedThe 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

Countries

United States

Participant flow

Recruitment details

December 2008 - August 2010

Participants by arm

ArmCount
Memantine
10-30mg tablets of memantine taken once daily by mouth
10
Total10

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyLost to Follow-up1

Baseline characteristics

CharacteristicMemantine
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
10 Participants
Age, Continuous32 years
STANDARD_DEVIATION 12.4
Region of Enrollment
United States
10 participants
Sex: Female, Male
Female
9 Participants
Sex: Female, Male
Male
1 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 10
serious
Total, serious adverse events
0 / 10

Outcome results

Primary

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

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

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

Population: Reported scores are Mean and standard deviation for Subjects last visit (Week 8 or last-observation carried forward).

ArmMeasureValue (MEAN)Dispersion
MemantineYale Brown Obsessive Compulsive Scale Modified for CB (CB-YBOCS)22 units on a scaleStandard Deviation 4

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026