NCT00676429

Ziprasidone for Severe Conduct and Other Disruptive Behavior Disorders

Ziprasidone for Severe Conduct and Other Disruptive Behavior Disorders in Children and Adolescents - a Placebo Controlled, Randomized, Double Blind Clinical Trial

• Status: Completed
• Phase: Phase 2
• Study type: Interventional
• Enrollment: 51 (actual)
• Sponsor: University Hospital Freiburg · Academic / Other
• Sex: All
• Age: 7 Years – 17 Years
• Healthy volunteers: Not accepted

Summary

To investigate and compare the efficacy, safety and tolerability of ziprasidone versus placebo in the treatment of conduct disorder (CD), oppositional defiant disorder (ODD) and disruptive behavior disorder not otherwise specified (DBD-NOS) of older children and adolescents in an outpatient setting. Conduct and other behavior disorders are some of the most common forms of psychopathology in children and adolescents. The main characteristic of these disorders is a repetitive and persistent pattern of antisocial, aggressive or defiant behavior that involves major violations of age-appropriate expectations or norms. According to the guidelines of the German Society for Child \& Adolescent Psychiatry \& Psychotherapy (Deutsche Gesellschaft für Kinder- und Jugendpsychiatrie und -psychotherapie DGKJPP), the European Society for Child and Adolescent Psychiatry (ESCAP), and the American Academy of Child and Adolescent Psychiatry (AACAP) currently no standard pharmacotherapy is established and recommended for children and adolescents. However Risperidone has been shown to be effective in the treatment of patients with disruptive behavior disorders and below average IQ.

Detailed description

Trial Design: A placebo-controlled, parallel-group, randomized, double-blind, single center design that includes a 3-weekly baseline period for finding the best individual dose, a 6-weeks treatment period and a 2-weeks washout period. Study Agent / Placebo - Dosage and Route of Administration: Study medication will first be dispensed at Visit 2 (day 1). Treatment assignments will be made in accordance with the randomization sequence. At each medication visit (Visit 2 to Visit 7), subjects will receive one bottle for the following week (Visit 2 to Visit 4) resp. the following two weeks (Visit 5 to Visit 7). Only qualified personnel may dispense study medication. The study population will be randomized equally to the verum or placebo group at Visit 2. All patients will receive an initial oral course starting with 5mg/d Ziprasidone Hydrochloride or placebo for patients with a body weight ≤ 50 kg and 10 mg/d Ziprasidone Hydrochloride or placebo for patients with a body weight \> 50 kg for the first week in the study. At Visit 3 the therapist can increase the dose to the double of the initial dose according to clinical response and tolerability. At Visit 4 the dose can be increased to the double of the last dose or reduced to the initial dose. At Visit 5 the most effective and best tolerated dose will be given for the 6 week fixed dose phase of the trial. Therefore the maximum daily dose is 20 mg (patients with body weight ≤ 50 kg) or 40 mg (patients with body weight \> 50 kg). The total dose will be split and the half-dose will be given twice a day (morning and evening). Planned Study Time Schedule: The study ends 11 weeks after enrollment of the last patient (total study end). Study duration for each patient is 11 weeks (from inclusion) until the last visit (close-out visit). Patients with a pre-treatment of psychotropic drugs will have an individual washout period before inclusion to the study. This individual washout period will last 5 elimination half-life of the taken drug. After randomization the patients will enter a 3 week dose escalation phase with weekly visits. Then a 6 week stable drug dose phase will follow with visits every second week, followed by a two week washout period and a final visit. Statistics: Sample size calculation: Sample size calculation is based on the assumption that treatment with Ziprasidone will show an effect size of ES=1 compared to treatment with placebo. In order to demonstrate this difference at a significance level of 5% and a power of 80%, 17 patients per group are required, and a drop-out rate of approximately 8 patients per group (with no data available to be analyzed according to the intention-to-treat principle) must be accounted for. Analysis of efficacy: The trial will be analyzed according to the intention-to-treat principle. The effect of treatment with Ziprasidone will be assessed by analyzing changes in the score of the scale described above. Changes calculated from the evaluations before and after treatment will be analyzed by means of analysis of covariance, considering the baseline measurement as a covariate. The difference between treatment groups will be estimated with a 95% confidence interval and will be tested within this model by the corresponding two-sided test at the 5% level of significance. Analysis of safety: Safety analyses will be performed for patients who received at least one dose of the investigational drug. Rates of adverse events and of serious adverse events will be calculated with corresponding 95% confidence intervals.

Conditions

• Conduct Disorder
• Oppositional Defiant Disorder

Interventions

Type	Name	Description
DRUG	Ziprasidone Hydrochloride	Ziprasidone Hydrochloride oral solution, individual titration 5 mg o.d. or 10 mg to 40 mg b.i.d
DRUG	Placebo	Placebo as oral solution, individually titrated

Timeline

• Start date: 2006-07-01
• Primary completion: 2008-06-01
• Completion: 2008-06-01
• First posted: 2008-05-13
• Last updated: 2008-11-18

Locations

1 site across 1 country: Germany