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A short treatment study of aripiprazole in pediatric patients with schizophrenia

A multicenter, double-blind, randomized, dose-comparison study of three different doses of aripiprazole orally administered over 6 weeks in pediatric patients with schizophrenia

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080221112
Enrollment
99
Registered
2010-05-27
Start date
2010-05-27
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizophrenia

Interventions

Sponsors

Otsuka Pharmaceutical Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients with a diagnosis of schizophrenia according to DSM-IV-TR 2) Male and female patients aged 13-17 years 3) Inpatient or outpatient status

Exclusion criteria

Exclusion criteria: 1) Patients who have a diagnosis of any other disease except schizophrenia according to DSM-IV-TR 2) Patients who fall under a contraindication listed in the ABILIFY package insert

Design outcomes

Primary

MeasureTime frame
PANSS total sore change from baseline in final judgement

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026