Effectiveness of Atypical Antipsychotic Medication for Outpatients With Anorexia Nervosa

Phase 4

Completed

Conditions: Eating Disorders

Interventions: Drug: Olanzapine
Drug: Aripiprazole

Registration Number: NCT00685334

Lead Sponsor: New York State Psychiatric Institute

Brief Summary: This study will compare the effectiveness of two atypical antipsychotic medications, olanzapine and aripiprazole, in treating people with anorexia nervosa.

Detailed Description: Anorexia nervosa (AN) is a disease of disordered eating that is characterized by self-starvation, often leading to extreme weight loss and difficulty maintaining a normal weight. Symptoms and behaviors of AN may include distorted body image, obsessive exercise, lack of menstruation among women, binge and purge eating behaviors, and intense fear of weight gain. Furthermore, people with AN are at a high risk of other mental disorders, such as depression and anxiety, and medical complications, such as organ damage, heart failure, and osteoporosis. Current treatments for AN include nutrition counseling, psychotherapy, and medication. Previous studies have suggested that certain medications usually used to treat schizophrenia, also known as atypical antipsychotic drugs, may be helpful in treating people with AN. Specifically, the atypical antipsychotic medications olanzapine and aripiprazole may be effective in improving overall symptoms of AN and in restoring weight to normal levels. This study will compare the effectiveness of olanzapine and aripiprazole in treating people with AN.

Participation in this study will last 12 weeks. All participants will first undergo baseline assessments that will include questionnaires and interviews about AN symptoms, a physical exam, vital sign measurements, an electrocardiograph (EKG), and a blood draw. Participants will then be assigned randomly to 12 weeks of treatment with daily olanzapine or aripiprazole. Participants will meet with a study doctor weekly over the 12 weeks of treatment. During these visits, the study doctor will monitor participants' progress, medication dosage, vital signs, and side effects. In addition, participants will undergo repeat blood draws every 4 weeks and repeat questionnaires every month of the treatment period. Upon completing the 12 weeks of treatment, participants will repeat most baseline assessments.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 22

Inclusion Criteria

Meets DSM-IV criteria for AN (DSM-IV criteria for amenorrhea will not be strictly applied, as these patients have been shown to be clinically indistinguishable from those with full criteria AN)
Body mass index (BMI) less than 19 kg/m2 and greater than 14 kg/m2 (BMI of 19 is equivalent to approximately 85% of ideal body weight [IBW] according to Metropolitan Life standards, and BMI of 14 is equivalent to approximately 65% IBW)
Unwilling to pursue inpatient treatment if BMI is less than 18 kg/m2
Free of psychotropic (e.g., antidepressant, antianxiety, mood stabilizer, antipsychotic) medication for 2 weeks before study entry (free for 4 weeks before study entry if taking fluoxetine or antipsychotic medications)
Prior treatment of AN

Exclusion Criteria

Any medical or psychiatric problem requiring urgent clinical attention (e.g., metabolic disturbance, acute suicidality) and/or significant comorbid illnesses that are not likely to benefit from proposed treatments
Significant orthostatic high blood pressure (systolic change greater than 30 mmHg upon changing from supine to standing position)
Allergy to olanzapine or aripiprazole
Commencing psychotherapy in the community within 3 months of study entry
Diabetes mellitus, with fasting serum glucose greater than 120 mg/dL or nonfasting serum glucose less than 140 mg/dL
Known history of current or past jaundice
Known history of narrow angle glaucoma
Active substance abuse or dependence
Schizophrenia, schizophreniform disorder, or bipolar illness
Movement disorder or presence of tics
History of tardive dyskinesia
History of seizures
Pregnant

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Olanzapine	Participants will take olanzapine
2	Aripiprazole	Participants will take aripiprazole

Primary Outcome Measures

Name	Time	Method
Tolerability	Measured at Week 12	This study addressed the benefits, tolerability, acceptability, safety, and appropriate dosage of olanzapine and aripiprazole, as determined by clinical evaluation and self report. The outcome measure reported here is the number of patients who did not experience untoward side effects while taking the medication.
Change From Baseline in Weight (Lbs.) at 12 Weeks	baseline and 12 weeks	This study looked at change in weight before and after medication use.

Secondary Outcome Measures

Name	Time	Method
Medication Side Effects	Measured at Week 12	Common side effects include sedation, dizziness, and headache for patients on olanzapine and akathisia, anxiety, dizziness and blurred vision for patients receiving aripriprazole.
Treatment Compliance	Measured at Week 12	Total number of randomized patients that completed the full 12 weeks of treatment.