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SchizophreniaPhase 4NCT05322031

The Impact of Aripiprazole Long-acting on Myelin and Cognition in the Onset of Schizophrenia

A Phase 4 study testing Aripiprazole in people with Schizophrenia and Myelin Degeneration, run by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico at 1 site in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The general objective of this interventional study is to explore the impact of long-acting arpiprazole on brain structure, in particular potential neurotrophic effects, neurogenetic and neuroprotective that could counteract the progressive neuronal degeneration inherent in the schizophrenic pathology itself. Read more about this study

Who is it for?
Ages 18 to 65 years
What is being tested?
Aripiprazole
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
1 siteItaly
Study dates
1 Aug 2022to 30 Nov 2024
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • onset of schizophrenia diagnosed by the support of structured clinical interview (SCID-5 CV) by specialized medical staff;
  • age 18 to 65 years, who, after a period of stabilization with aripiprazole in oral formulation, must start a therapy with long-acting aripiprazole for clinical needs (and therefore regardless of participation in the study) or already in therapy with long-acting aripiprazole not more than two weeks;
  • absence of other psychotropic drugs for at least two weeks prior to the start of the study;
  • to have signed the informed consent to participate in the study;
  • for women of child-bearing age, a pregnancy test (betaHCG urine or blood test) must be carried out immediately before the start of therapy and a highly effective method of contraception must be taken for the duration of the treatment.

Who cannot join

  • presence of codiagnosis with other psychiatric (based on SCID-5 CV) or neurological pathologies;
  • previous antipsychotic therapies. Patients previously stabilized with other antipsychotic drugs will still be admitted, provided that they are taken for a period of time not exceeding one month and provided that they have not been taken within 2 weeks prior to enrollment, except for aripiprazole in oral formulation, the intake of which is necessary for the inclusion of aripiprazole in long-acting formulation.
  • contraindications to taking aripiprazole long-acting as per SPC;
  • history of intellectual disability;
  • abuse of alcohol or substances during the preceding six months;
  • presence of absolute or relative contraindications to the execution of MRI;
  • underage patients;
  • pregnant women (if the pregnancy occurs during the study, the patient will be excluded from the continuation of the study) or women who have not performed a pregnancy test negative result before the start of therapy and who do not adopt valid contraceptive methods.

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • Prof. Paolo Brambilla

    Milan, Italy, 20100

Other trials in Italy

About this study

The general objective of this interventional study is to explore the impact of long-acting arpiprazole on brain structure, in particular potential neurotrophic effects, neurogenetic and neuroprotective that could counteract the progressive neuronal degeneration inherent in the schizophrenic pathology itself.

Each subject will undergo a structured clinical interview to assess the presence/absence of Axis I psychiatric disorders (SCID-5 CV). This evaluation is carried out in common clinical practice as a tool to support diagnosis in patients with suspected schizophrenia.

Read more

In all subjects, the cognitive profile will be evaluated through the Brief Assessment of Cognition in schizophrenia (BAC-S). The degree of psychotic symptomatology reported through the administration of specific psychopathological scales such as the Brief Psychiatric Rating Scale (BPRS) and the Positive and Negative Syndrome Scale (PANSS) will also be measured. Further clinical data will be extrapolated from medical records and interviews with psychiatrists, if available.

In patients diagnosed with schizophrenia at the first psychotic episode, the administration of pharmacological therapy with long-acting aripiprazole will take place following the indications of the relevant data sheet.

At the U.O.C. of Neuroradiology of the Fondazione, all enrolled subjects will undergo a 3-Tesla multimodal neuroimaging session that includes:

  • T1-weighted sequences: to study the volumetric differences of white and grey matter between subjects before and after treatment;
  • Acquisition of myelin sequences: to assess the differences in myelin between subjects before and after treatment;
  • DTI sequences: to assess differences in white matter bundles between subjects before and after treatment.

The degree of psychotic symptomatology reported will be evaluated by the repetition of psychopathological scales (BPRS, PANSS). Three months after the start of therapy all patients who have joined the study will carry out a 3T NMR of extra standard care control.

Read the detailed description

The general objective of this interventional study is to explore the impact of long-acting arpiprazole on brain structure, in particular potential neurotrophic effects, neurogenetic and neuroprotective that could counteract the progressive neuronal degeneration inherent in the schizophrenic pathology itself. In other words, the primary objective is to assess if the achievement of therapeutic control of the pathology through the use of antipsychotic drug corresponds to a change in the brain structure, both in terms of morphology and connectivity. A further objective will be to evaluate the effect of long-acting aripiprazole on the clinical outcome (in terms of relapses and clinical symptoms), on the overall functioning and cognitive performance of patients at the first psychotic episode in the context of a diagnosis of schizophrenia. The study will be attended by patients with onset of schizophrenia recruited from the Psychiatric Service of Diagnosis and Care and the Day Hospital of the U.O.C. of Psychiatry of the IRCCS Fondazione Ca' Granda, Ospedale Maggiore Policlinico in Milan. A team of psychologists and medical experts of the UOC of Psychiatry of the Fondazione will conduct the process of enrollment and participation in the study. Each subject will undergo a structured clinical interview to assess the presence/absence of Axis I psychiatric disorders (SCID-5 CV). This evaluation is carried out in common clinical practice as a tool to support diagnosis in patients with suspected schizophrenia.

In all subjects, the cognitive profile will be evaluated through the Brief Assessment of Cognition in schizophrenia (BAC-S). In patients, the degree of psychotic symptomatology reported through the administration of specific psychopathological scales such as the Brief Psychiatric Rating Scale (BPRS) and the Positive and Negative Syndrome Scale (PANSS) will also be measured. Further clinical data will be extrapolated from medical records and interviews with psychiatrists, if available.

In patients diagnosed with schizophrenia at the first psychotic episode, the administration of pharmacological therapy with long-acting aripiprazole will take place following the indications of the relevant data sheet, upon prescription of the doctor, on the basis of the clinical assessment and independently of participation in the study. The introduction of aripiprazole long-acting drug therapy will follow a period of stabilization with oral aripiprazole, as reported in the data sheet.

At the U.O.C. Neuroradiology of the Fondazione, all enrolled subjects will undergo a 3-Tesla multimodal neuroimaging session that includes:

  • T1-weighted sequences: to study the volumetric differences of white and grey matter between subjects before and after treatment;
  • Acquisition of myelin sequences: to assess the differences in myelin between subjects before and after treatment;
  • DTI sequences: to assess differences in white matter bundles between subjects before and after treatment.

This resonance is an ordinary clinical practice for patients with psychosis. It is important to note that 3T MRI is no longer considered high-field and is now commonly used in the regular clinical practice.

For patients, clinical reassessment visits (one per month for 3 months) are already scheduled by practice for the normal management of the clinical situation. The degree of psychotic symptomatology reported will be evaluated by the repetition of psychopathological scales (BPRS, PANSS). Three months after the start of therapy all patients who have joined the study will carry out a 3T NMR of extra standard care control.

Being tested
Aripiprazole
Keywords
Onset of schizophrenia, Aripiprazole long-acting, Myelin, Cognition
Medical subject headings
Schizophrenia, Cognition Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AripiprazoleDrug

    Also called Abilify Maintena, Long-acting aripiprazole

    Patiens who underwent a a period of stabilization with aripiprazole in oral formulation that begin therapy with long-acting aripiprazole, or already in therapy with long-acting aripiprazole from no more than two weeks.

Study groups in NCT05322031
Study groupRoleWhat they receive
Onset of depressionExperimental15 participants with onset of schizophrenia who, after a period of stabilization with aripiprazole in oral formulation, would begin therapy with long-acting aripiprazole, or already in therapy with long-acting aripiprazole since no more than two weeks.
Receives: Drug: Aripiprazole

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Brain structural modifications in terms of myelination of the white matter measured using magnetic resonance imaging

    Evaluation of the modification of the myelination of white matter bundles (in terms of Myelin Water Fraction - MWF) after antipsychotic therapy with aripiprazole long-acting compared to baseline measured using magnetic resonance imaging.

    Measured: 3 months of therapy

Secondary outcomes (8)
  1. Evaluation of efficacy as assessed by Positive and Negative Syndrome scale

    Evaluation of the efficacy of aripiprazole long-acting on the clinical outcome, measured by variation of the score of the psychopathological PANSS (Positive and Negative Syndrome Scale) scale with respect to the baseline.

    Measured: 3 months from baseline.

  2. Evaluation of efficacy as assessed by Brief Psychiatric Rating Scale

    Evaluation of the efficacy of aripiprazole long-acting on the clinical outcome, measured by variation of the score of the psychopathological BPRS (Brief Psychiatric Rating Scale) scale with respect to the baseline.

    Measured: 3 months from baseline.

  3. Changes in cognitive performance through Brief Assessment of Cognition in schizophrenia scale

    Evaluation of the efficacy of aripiprazole long-acting on the cognitive performance, measured in terms of variations of neuropsychological BAC-S (Brief Assessment of Cognition in schizophrenia) scale scores with respect to the baseline

    Measured: 3 months from baseline.

  4. Number of adverse and toxic events due to the administration of aripiprazole

    Evaluation of serious and non-serious adverse and toxic events due to the administration of aripiprazole.

    Measured: Through study completion (1 year)

  5. Evaluation of the statistical correlation between plasma levels of aripiprazole and clinical and structural assestment

    Assessment of the plasma levels over time of the drug to identify a possible statistical correlation with the clinical response (in terms of changes with respect to the baseline in PANSS - Positive and Negative Syndrome Scale, BAC-S - Brief Assessment of Cognition in schizophrenia and BPRS - Brief Psychiatric Rating Scale) and with the changes in brain structure (in terms of gray matter volumes, superficial cortical area and cortical thickness) and in the myelination of white matter bundles (in terms of Myelin Water Fraction - MWF).

    Measured: Through study completion (1 year)

  6. Changes in gray matter volumes

    Evaluation of changes in brain structure using MRI in terms of gray matter volumes after antipsychotic therapy with long-acting aripiprazole.

    Measured: 3 months from baseline

  7. Changes in superficial cortical area

    Evaluation of changes in brain structure using MRI in terms of superficial cortical area after antipsychotic therapy with long-acting aripiprazole.

    Measured: 3 months from baseline

  8. Changes in cortical thickness

    Evaluation of changes in brain structure using MRI in terms of cortical thickness after antipsychotic therapy with long-acting aripiprazole.

    Measured: 3 months from baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Apr 2022
  2. Study start1 Aug 2022
  3. Primary completion31 Aug 2024
  4. Study completion30 Nov 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
15 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05322031
Sponsor's protocol ID
ARIANNA
Status last verified
Oct 2024
First submitted
16 Mar 2022
Last updated
27 Dec 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Aripiprazole in people with Schizophrenia and Myelin Degeneration, run by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Dec 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Brain structural modifications in terms of myelination of the white matter measured using magnetic resonance imaging (time frame: 3 months of therapy). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Dec 2024.

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