SWITCH: Observational Study on the Effect of Switch to Lurasidone in Subjects With Schizophrenia"

Sponsor
Aziende Chimiche Riunite Angelini Francesco S.p.A (Industry)
Overall Status
Recruiting
CT.gov ID
NCT04312503
Collaborator
(none)
300
15
29.6
20
0.7

Study Details

Study Description

Brief Summary

The aim of this study is observation, in an Italian real-world setting, of metabolic effects in patients with schizophrenia who will switch from any mono-therapy or poly-therapy antipsychotic regimen to monotherapy with lurasidone or to one of the other four most used atypical antipsychotics.

Condition or Disease Intervention/Treatment Phase

Detailed Description

The aim of this study is the observation, in psychiatric Italian real-world settings, of metabolic effects, effectiveness, side effects and therapeutic adherence in patients with schizophrenia who switched, for any reason (efficacy, safety, metabolic problems, therapeutic adherence or patient's request), from any mono-therapy or poly-therapy antipsychotic regimen to monotherapy with lurasidone or with one of the four most used atypical antipsychotics in Italy (aripiprazole, olanzapine, quetiapine, risperidone). Patient's past medical and psychiatric history of the last 12 months will be also evaluated.

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Observational Study on the Effect of Switch to Lurasidone or Other Antipsychothics on Metabolic and Weight Changes in Subjects With Schizophrenia"
Actual Study Start Date :
Jul 13, 2020
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
COHORT A: Lurasidone

Patients treated with Lurasidone

Drug: Lurasidone
Patients are treated with dosages according clinical practice
Other Names:
  • Latuda
  • COHORT B: aripiprazole, olanzapine, quetiapine or risperidone)

    Patients treated with other atipical antypsicothic as aripiprazole, olanzapine, quetiapine or risperidone)

    Drug: aripiprazole, olanzapine, quetiapine or risperidone
    Patients are treated with dosages according clinical practice

    Outcome Measures

    Primary Outcome Measures

    1. Change in the metabolic parameters [4 weeks]

      Change in metabolic syndrome in 3 of 5 parameters: Arterial hypertension defined as. systolic pressure ≥ 130 mmHg and/or diastolic pressure ≥85 mmHg or treatment for hypertension. Waist Circumference ≥ 90 cm in men or ≥ 80 cm in women. Fasting Plasma Glucose ≥5.6 mmol/l and/or known treatment for hyperglycemia. Triglycerides ≥1.7 mmol/l or medication for elevated triglycerides. HDL Cholesterol ≤ 1.0 mmol/l in men and ≤1.3 mmol/l for women or taking medication.

    Secondary Outcome Measures

    1. Retrospective investigation of the metabolic effects of switches to any atypical antipsychotic occurred in the previous 12 months [12 months before baseline (switch to any atypical antipsychotics)]

      Change in metabolic syndrome in 3 of 5 parameters: Arterial hypertension defined as. systolic pressure ≥ 130 mmHg and/or diastolic pressure ≥85 mmHg or treatment for hypertension. Waist Circumference ≥ 90 cm in men or ≥ 80 cm in women. Fasting Plasma Glucose ≥5.6 mmol/l and/or known treatment for hyperglycemia. Triglycerides ≥1.7 mmol/l or medication for elevated triglycerides. HDL Cholesterol ≤ 1.0 mmol/l in men and ≤1.3 mmol/l for women or taking medication.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with a diagnosis of schizophrenia according to DSM-5.

    • Patients who gave their written consent for participation in the study and for personal data processing and willing to comply with all study procedures.

    • Male and female patients ≥ of 18 years old at baseline.

    • Patients treated or in treatment with any typical or atypical antipsychotic monotherapy or polytherapy.

    • Patients switched from the pre-existing therapy to lurasidone, aripiprazole, olanzapine, quetiapine or risperidone in monotherapy within the preceding 2 weeks. The date of the switch is considered as baseline.

    Exclusion Criteria:
    • Female patients who are pregnant or lactating

    • Patients fulfilling DSM-5 criteria for diagnosis of bipolar disorder and/or dementia.

    • Amphetamines and/or Opiates abuse or dependence , as defined by DSM-5 criteria.

    • Patients with no history of antipsychotics use.

    • Patients recruited in another study as follows:

    • currently enrolled in any pharmacological or non-pharmacological, interventional or observational study:

    • who participated in the last 30 days to any observational or no-profit interventional study;

    • who participated in the last 12 months to any interventional commercially sponsored study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ospedali Riuniti SOD di Clinica Psichiatrica Ancona AN Italy 60126
    2 Spedali Civili di Brescia Dipartimento di Salute Mentale 1 Brescia BS Italy 25123
    3 A.O.U. di Cagliari Corso Vittorio Emanuele II, 6 09124 Cagliari (CA) Cagliari CA Italy 09124
    4 P.O. Gaspare Rodolico - U.O.C. di Psichiatria Catania CT Italy 95125
    5 AO Mater Domini U.O. Psichiatria Catanzaro CZ Italy 88100
    6 A.O.U. Ospedali Riuniti di Foggia - S.P.D.C. Viale Pinto 71121 Foggia (FO) Foggia FG Italy 71121
    7 DSM Dipartimento Salute Mentale Lecce LE Italy 73100
    8 Ospedale S. Gerardo Università Bicocca Dipartimento di Salute Mentale Monza MB Italy 209900
    9 Ospedale Maggiore Policlinico di Milano U.O. C. di Psichiatria Milan MI Italy 20122
    10 Ospedale San Raffaele U.O.C. Psichiatria Generale e Riabilitazione Milan MI Italy 20127
    11 Ospedale Luigi Sacco, S.C. Psichiatria 2 Milan MI Italy 20157
    12 III S.P.D.C. Azienda Ospedaliera di Padova 35128 Padova - (PD) Padova PD Italy 35128
    13 Clinica Von Sibenthal Via della Madonnina, 1 Genzano Di Roma RM Italy 00045
    14 A.O.U. San Luigi Gonzaga - S.C.D.U. di Psichiatria Regione Gonzole, 10 Orbassano TO Italy 10043
    15 Azienda Ospedaliera - Universitaria Senese Siena Italy 53100

    Sponsors and Collaborators

    • Aziende Chimiche Riunite Angelini Francesco S.p.A

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Aziende Chimiche Riunite Angelini Francesco S.p.A
    ClinicalTrials.gov Identifier:
    NCT04312503
    Other Study ID Numbers:
    • 151(A)PO18531
    First Posted:
    Mar 18, 2020
    Last Update Posted:
    Jul 20, 2022
    Last Verified:
    Mar 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Aziende Chimiche Riunite Angelini Francesco S.p.A
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 20, 2022