ARIpiprazole in Anorexia NErvosa
- Registration Number
- NCT01082848
- Lead Sponsor
- Juan A. Arnaiz
- Brief Summary
Evidence is lacking on the effects of different psychotropic drugs in the treatment of anorexia nervosa (AR). However, HVA levels seem to be elevated in this disease, therefore suggesting a role for drugs with a partial agonist profile on dopaminergic receptors. This is a pilot study assessing the effects of aripiprazole in teenagers with AR, compared with a placebo.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
- age between 12 and 18
- diagnostic criteria for anorexia Nervosa (DSM-IV-TR (includes BMI below 17.5kg/m2 and above 14 kg/m2) confirmed by a Psychiatrist and validated by K-SADS-PL interview
- severity criteria requiring Hospital admission
- Consent given by parents and patients
Exclusion Criteria
- psychotic illness
- antipsychotic therapy at inclusion
- pregnancy and breastfeeding
- antipsychotic drug allergy
- prior head trauma, malignant neuroleptic syndrome or epilepsy
- relevant comorbidities requiring therapy
- detection of abuse drugs in urine test
- treatment with neuroleptic, antidepressant or mood stabilizers during 2 weeks prior to randomization (4 weeks in case of fluoxetine)
- suicidal or homicidal thoughts
- IQ below 70
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description aripiprazole aripiprazole - placebo placebo -
- Primary Outcome Measures
Name Time Method Eating Disorder Inventory-2 6 months Eating attitudes test (EAT) 6 months Brown Assessment of Beliefs Scale (BABS) 6 months
- Secondary Outcome Measures
Name Time Method BMI 6 months Body mass index
BDI 6 months Beck Depression Inventory
Trial Locations
- Locations (1)
Hospital Clinic
🇪🇸Barcelona, Catalonia, Spain