N-acetylcysteine in Bulimia Nervosa
- Registration Number
- NCT01131572
- Lead Sponsor
- Lindner Center of HOPE
- Brief Summary
This study tests NAC in the treatment of Bulimia Nervosa.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 11
Inclusion Criteria
- Bulimia Nervosa
- 18-65 years of age
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description N-acetylcysteine N-acetylcysteine NAC open label treatment. Each subject receives N-acetylcysteine.
- Primary Outcome Measures
Name Time Method Binge-purge episodes per week The primary outcome measure will be the weekly frequency of binge-purge episodes. A binge-purge eating episode will be defined using DSM-IV-TR criteria, and accessed via clinical interview and review of subject take-home diaries at each study visit.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie N-acetylcysteine's efficacy in Bulimia Nervosa treatment?
How does N-acetylcysteine compare to SSRIs in treating Bulimia Nervosa symptoms and relapse rates?
Are there specific biomarkers that predict response to N-acetylcysteine in eating disorder patients?
What adverse events are associated with N-acetylcysteine in phase 2 trials for Bulimia Nervosa?
What combination therapies with N-acetylcysteine show promise in treating Bulimia Nervosa?
Trial Locations
- Locations (1)
Lindner Center of HOPE
🇺🇸Mason, Ohio, United States
Lindner Center of HOPE🇺🇸Mason, Ohio, United States