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Effectiveness of switching to aripiprazole long-acting injection from other long-acting injections and oral antipsychotics in patients with schizophrenia

Effectiveness of switching to aripiprazole long-acting injection from other long-acting injections and oral antipsychotics in patients with schizophrenia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010280
Enrollment
212
Registered
2025-03-11
Start date
2024-10-10
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

None listed

Interventions

Drug : - Aripiprazole Monohydrate(Abilify Maintena Inj) : 300mg or 400mg , used an an IM injection into the deep deltoid or gluteus musche, 4Week intervals. - The switch to aripiprazole long-acting in

Sponsors

Chonnam National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Diagnosed with schizophrenia utilizing the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) ? Male or female patients who are 19-65 years(inclusive) of age at time of consent ? Patients maintained on current Other dopamine antagonists such as oral or LAI antipsychotics other than Aripiprazole for more than 2 weeks and those should have such as problems efficacy, tolerability, or compliance, per physician judgement or patient's report ? Patients must be fluent in the language of the questionnaires and cooperate in the study ? Patients must be capable of providing signed and dated written informed consent and fully understand the purpose of the study

Exclusion criteria

Exclusion criteria: ? Patients who have current or previous clinically significant findings of physical illness ? Patients with significant suicide risk ? Women who are pregnant, nursing ? Patients with severe drug allergy and severe side effects ? Currently receiving oral aripiprazole monotherapy ? Patients who are participating in drug trials

Design outcomes

Primary

MeasureTime frame
Subjective Wellbeing under Neuroleptics-short form

Secondary

MeasureTime frame
Social and Occupational Functioning Scale;Positive and Negative Syndrome Scale

Countries

Korea, Republic of

Contacts

Public ContactAnna Jo

Chonnam National University Hospital

dksskrha@hanmail.net+82-62-220-5270

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026