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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02138058
Other study ID # Topiramate for oniomania
Secondary ID
Status Completed
Phase Phase 2
First received May 12, 2014
Last updated May 8, 2017
Start date January 2015
Est. completion date June 2016

Study information

Verified date December 2015
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It is a double blind controlled study to test the hypothesis that Topiramate is more effective than placebo in the treatment of compulsive buying, during a period of 12 weeks


Description:

Compulsive buying is a prevalent disorder with no approved pharmacological treatment. Previous reports suggest that topiramate could be useful in reducing impulsivity in pathological gambling and other impulse control disorders, as well as craving in substance addictions. The goal of this study was to investigate the effectiveness of topiramate combined with brief cognitive restructuring in treating compulsive buying, compared with just cognitive restructuring treatment+placebo.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date June 2016
Est. primary completion date June 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 60 Years
Eligibility Inclusion Criteria:

- Match criteria for compulsive buying, according to McElroy et al. (1994), confirmed by semi-structured interview modeled after the Schedules for clinical assessment in neuropsychiatry (SCID)

- woman within fertility age have to be already practicing an acceptable contraception method and to be negative at a pregnancy test

Exclusion Criteria:

- illiteracy

- pregnancy and breastfeeding for woman

- previous history of alcohol abuse/dependence with current elevation of liver enzymes, or a present diagnosis of alcohol abuse/dependence

- past or current drug abuse/dependence, except for nicotine

- history of current or past Fifth Edition of the Diagnostic and Statistical Manual of Mental Disorders diagnosis of bipolar disorder, schizophrenia, psychosis or any neuropsychiatric condition causing cognitive impairment

- a history of suicide attempt or acute suicide risk

- severe depression indicated by a score higher than 30 at the beck depression inventory

- current participation on psychotherapy or use of pharmacological agent or experimental dispositive for compulsive buying in the past 3 months

- current use of psychotropic drugs, except benzodiazepines

- cardiovascular disease including a history of heart attack, stroke, arrhythmia, cardiac failure in the past 5 years. Uncontrolled high blood pressure.

- chronic or acute renal or liver failure, as well as Retinopathy and thyroidopathy

- a personal or family history of nephrolithiasis

- immunodeficiency

- any blood dyscrasia

- contraindication or allergy to topiramate

- history of seizures

- dont't have a phone number for contact

- live alone and don't have a person that can inform about the shopping behavior

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Topiramate

Behavioral:
Cognitive restructuring intervention
4 sessions of a manualized cognitive restructuring intervention for compulsive buying

Locations

Country Name City State
Brazil Associação Viver Bem São Paulo SP

Sponsors (1)

Lead Sponsor Collaborator
University of Sao Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Other Social adjustment The social Adjustment scale (SAS) is a self-report scale that assesses seven specific areas: work, social, life and leisure, extended family relationship, marital relationship, relationship with offsprings, domestic life and financial situation 12 weeks
Primary Yale-Brown Compulsive-Obsessive Scale Shopping Version It is a revised version of the Yale-Brown Obsessive-Compulsive Scale (YBOCS), created to assess both the cognitive and behaviour of compulsive buying as well as to rate the severity of the problem 12 weeks
Secondary Clinical Global Impression scale (CGI) The CGI scale quantifies the severity of disease and the effects of treatment, as well as overall clinical improvement. 12 weeks
Secondary Udvalg for KliniskeUndersøgelser Side Effect Rating Scale (UKU) It was developed to provide a comprehensive side effect rating scale with well-defined and operationalized items to assess the side effects of psychopharmacological medications. 12 weeks
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