Topiramate Augmentation in Bulimia Nervosa Partial Responders

Status Withdrawn

Clinical Trial Summary

The goal of this study is to generate pilot data exploring the addition of an augmentation (additional) medication to patients suffering from bulimia nervosa who have responded but not had complete symptom resolution with a course of standard medication treatment.

Clinical Trial Description

The aim of this study is to determine whether the addition of an augmentation medication (topiramate 200mg/d) will confer additional reductions in symptomatology in BN patients who have received six weeks of standard pharmacological treatment with fluoxetine 60 mg/day or its equivalent and had a partial response but are not in symptomatic remission. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00988481
Study type	Interventional
Source	Neuropsychiatric Research Institute, Fargo, North Dakota
Contact
Status	Withdrawn
Phase	Phase 4
Start date	September 2009
Completion date	September 2010

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