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.
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
- Conditions the study is for
- Schizophrenia, Myelin Degeneration, Cognition Disorder
- 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.
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.
- Conditions
- Schizophrenia, Myelin Degeneration, Cognition Disorder
- 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 group | Role | What they receive |
|---|---|---|
| Onset of depression | Experimental | 15 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.
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)
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.
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.
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.
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)
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)
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
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
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.
- First posted11 Apr 2022
- Study start1 Aug 2022
- Primary completion31 Aug 2024
- Study completion30 Nov 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SchizophreniaStudies of the same condition, open and under way.
- More trials run by Fondazione IRCCS Ca' Granda, Ospedale Maggiore PoliclinicoThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Paolo Brambilla, Professor, Study chair, Fondazione IRCCS Ca' Granda, Ospedale Maggiore PoliclinicoMassimo C Mauri, Professor, Study director, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
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
Study at a glance
From the registry record, last updated by the sponsor on 27 Dec 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Impact of Aripiprazole Long-acting on Myelin and Cognition in the Onset of Schizophrenia
- ClinicalTrials.gov ID
- NCT05322031
- Acronym / sponsor ID
- ARIANNA
- Conditions
- Schizophrenia, Myelin Degeneration, Cognition Disorder
- Keywords
- Onset of schizophrenia, Aripiprazole long-acting, Myelin, Cognition
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 15 participants (actual)
- Lead sponsor
- Fondazione IRCCS Ca' Granda, Ospedale Maggiore PoliclinicoUniversity, hospital or other
- Study start
- 1 Aug 2022 (actual)
- Primary completion
- 31 Aug 2024 (actual)
- Study completion
- 30 Nov 2024 (actual)
- First posted
- 11 Apr 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Onset of depression | Experimental | Drug: Aripiprazole15 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. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- 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.
Key exclusion criteria (8 listed)
- 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;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| AripiprazoleAlso: Abilify Maintena, Long-acting aripiprazolePatiens 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. | Drug | Onset of depression |
Primary outcome
Brain structural modifications in terms of myelination of the white matter measured using magnetic resonance imaging
Time frame: 3 months of therapy
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.
8 secondary outcomes
Evaluation of efficacy as assessed by Positive and Negative Syndrome scale
Time frame: 3 months from baseline.
Evaluation of efficacy as assessed by Brief Psychiatric Rating Scale
Time frame: 3 months from baseline.
Changes in cognitive performance through Brief Assessment of Cognition in schizophrenia scale
Time frame: 3 months from baseline.
Number of adverse and toxic events due to the administration of aripiprazole
Time frame: Through study completion (1 year)
Evaluation of the statistical correlation between plasma levels of aripiprazole and clinical and structural assestment
Time frame: Through study completion (1 year)
Changes in gray matter volumes
Time frame: 3 months from baseline
Changes in superficial cortical area
Time frame: 3 months from baseline
Changes in cortical thickness
Time frame: 3 months from baseline
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Dec 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Paolo Brambilla, Professor study chair
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Massimo C Mauri, Professor study director
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
1 site in 1 country: see every site and its status.
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.