A randomized double-blind, placebo-controlled study of risperidone in the treatment of aggressive antisocial behavior in youth.

• Conditions: Conduct Disorder DSM-IV-TR; 312.8x¸ APA, 2000; MedDRA version: 16.0Level: PTClassification code 10064478Term: Conduct disorderSystem Organ Class: 10037175 - Psychiatric disorders; Therapeutic area: Psychiatry and Psychology [F] - Behavioral Disciplines and Activities [F04]

• Registration Number: EUCTR2011-000567-26-ES
• Lead Sponsor: Radboud University Medical Centre Nijmegen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-06-24
• Last Update Posted: 5 August 2013

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: 264

Inclusion Criteria

Inclusion Criteria:
1-Male or female patients, aged 5;0 - < 17;9 years at Visit 1.
2-Patients must have an IQ of > 85 (based on,> 4 subtests, 2 verbal plus 2 performance tests) from the Wechsler IQ Scales, e.g. WISC; WAIS; assessed within < 2 y. before or at study entry), e.g.: vocabulary, similarities, block design, and matrix reasoning (cf. Crawford et al., 2010). Age- and country-specific adaptations may be used (detailed instructions may be provided in a respective extra document).
3-Patients must meet diagnostic criteria for DSM-IV TR Conduct Disorder(s), as confirmed by the Kiddie-SADS, Conduct Disorder Module: 312.8x. (Kaufman et al., 1996), at Visit 2 or Visit 3.
4-Patients must score ? 27 on the Nisonger CBR Form, ODD/CD Disruptive Behavior Composite (D-Total) at Visit 2 or Visit 3.
5-Patients must score ?4 (?moderately ill?) on the CGI-S rating scale at Visits 2 and 3.
6-If a female of child-bearing potential, patients must test negative for pregnancy at the time of enrollment based on a serum pregnancy test and agree to use a reliable method of birth control. (Adequate contra- ception includes: oral contraceptives, intrauterine devices; double barrier method (diaphragm or condom plus spermicide), Norplant? or Depot Provera?).
7-Patients must have a body weight of at least 20 kg at study entry.
8-Patients must be able to swallow study drug.
9-Patients must have venous access sufficient to allow blood sampling and are compliant with blood draws as per protocol.
10-Subjects? parents/legal guardians must provide and sign informed consent documents; patients must provide informed consent, and sign consent or assent documents if capable, according to the legal requirements in the very country.
11-A reliable person (primary caregiver, parent) must be available to ensure compliance with study procedures throughout the course of the study.
12-Parents and patients must have a level of education, understanding and command of language suitable to adequately communicate with investigator and study coordinator.
13-Patients meeting criteria for comorbid ADHD (as to the clinical judgment of the investigator) will not be excluded from study participation.
Are the trial subjects under 18? yes
Number of subjects for this age range: 23
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1-Is immediate family of investigator site personnel directly affiliated with this study. Immediate family is defined as a spouse, parent, child, or sibling, whether biological or legally adopted.
2-Has been treated with a drug within 14 days before Visit 1 that has not received regulatory approval for any indication at the time of study entry.
3-Has participated in any investigational drug trial within six months prior to baseline (visit 3).
4-Has previously completed or withdrawn from this study or any other study investigating risperidone or has previously been identified as being a nonresponder or intolerant of risperidone.
5-In the clinical judgment of the investigator, has a current (within 6 months of the start of the study) or lifetime DSM-IV-TR diagnosis of schizophrenia-related disorders, schizophrenia, bipolar disorder, major depressive disorder, or current substance dependence disorder (given the nature of the study population substance misuse or abuse is not exlusionary), pervasive developmental disorder (autistic disorder or Asperger disorder).
6-In the clinical judgment of the investigator, currently meets criteria for a primary psychiatric disorder, e.g., Anxiety Disorder, Depressive Disorder, Tic Disorder or Tourette?s Syndrome (comorbid ADHD is permitted, cf. Incl. criteria section)
7-Starts any psychotropic medication, including health-food supplements that the investigator feels could have central nervous system activity (for example, St. John?s Wort, melatonin), during the course of the study, or is taking any other excluded concomitant medication(s) at/beyond Visit 2 (specified in Section 5.7). (An ongoing long-term medication, e.g., to treat a comorbid disorder such as ADHD, is permitted as long as compound and dose are not changed throughout the course of the study.)
Has any acute or unstable medical condition, physiological condition, clinically significant laboratory, or ECG results that, in the opinion of the investigator, would compromise participation in the study.
8-Has a known or suspected seizure disorder.
9-Has a history of neuroleptic malignant syndrome (NMS) or of tardive dyskinesia.
10-Has a history of severe allergies to medications, in particular hypersensitivity to neuroleptics, or of multiple adverse drug reactions.
11-Is pregnant or nursing.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified