Bulimia Nervosa Clinical Trial
Official title:
Qsymia (Phentermine-topiramate) to Reduce Binge Eating/Purging in Patients With Bulimia Nervosa and Binge Eating Disorder
This study will demonstrate the efficacy of Qsymia versus placebo in treating bulimia nervosa and binge eating disorder.
Bulimia nervosa (BN) and binge eating disorder (BED) are serious mental disorders associated
with adverse psychological and physical consequences. Treatment options to date offer limited
success, leaving at least 50-70% of patients still symptomatic after treatment. The purpose
of the study is to evaluate whether phentermine-topiramate (Qsymia), a medication currently
FDA approved for the treatment of obesity, will demonstrate efficacy—compared to placebo-
when re-purposed for patients with bulimia and binge eating.
Participants will be randomized into one of two conditions: qsymia or Placebo. One condition
will receive 3 months of phentermine-topiramate, a 2 week washout, then 3 months of placebo.
The other condition will receive 3 months of Placebo, a 2 week washout, then 3 months of
phentermine-topiramate. Participants will receive a total of 6 months of treatment and then
have a 2 month follow-up off of medications.
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