RecruitingPhase 4NCT05958875

The Effect of a Six Week Intensified Pharmacological Treatment for Schizophrenia Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment.

A Randomised, Controlled Trial to Investigate the Effect of a Six Week Intensified Pharmacological Treatment for Schizophrenia Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment.


Sponsor

Dr. Inge Winter

Enrollment

418 participants

Start Date

Aug 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Schizophrenia (SZ) affects approximately 4.5 million people across the European Union (EU) and is associated with annual healthcare and societal costs of 29 billion Euros. The impact on the daily life of patients is huge, ranging from frequent relapses and hospitalisations, the inability to maintain a job or continue scholing, to a low quality of life, impaired cognitive functioning, suicidal ideation and an increase morbidity rate, next to the large burden for carers 1. When diagnosed with schizophrenia or related disorder, patients are commonly prescribed antipsychotics. One-third of the schizophrenia patients are regarded treatment-resistant (TR), meaning that at least two antipsychotic trials have failed. Typically, clozapine is prescribed for TR patients, which is effective for approximately 40% of patients. Clozapine is among the most effective treatments, with the lowest all-cause mortality. Although it is among the most effective antipsychotics, it is generally not used earlier in the illness course due to a small risk of severe neutropenia/agranulocytosis, which is why patients treated with clozapine are intensely monitored. However, this small risk outweighs the burden of not receiving an effective treatment. Since clozapine is among the most effective treatments, this leads to the research question whether earlier initiation of third-line treatment ('early intensified' pharmacological treatment; EIPT) would be more beneficial than the current second-line treatments (treatment as usual; TAU). If this is indeed the case, this could lead to the prevention of unnecessary trials of ineffective treatments, hospitalisations, and recommendations for adaptations of worldwide guidelines as well as a reduction of healthcare and societal costs The INTENSIFY-Schizophrenia trial is part of the larger Horizon 2021 project Psych-STRATA, with the central goal of paving the way for a shift towards a treatment decision-making process tailored for the individual at risk for treatment resistance. To that end, the inestigators aim to establish evidence-based criteria to make decisions of early intense treatment in individuals at risk for treatment resistance across the major psychiatric disorders of schizophrenia, bipolar disorder and major depression. The current protocol focuses on the sample of schizophrenia patients.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether switching to an intensified drug regimen (including clozapine) more quickly after a treatment failure leads to better outcomes in people with schizophrenia, schizoaffective disorder, or schizophreniform disorder who are not responding to their current medication. **You may be eligible if...** - You are 18 to 70 years old with a diagnosis of schizophrenia, schizoaffective disorder, or schizophreniform disorder - Your current medication is not working well enough (confirmed by a clinical rating scale) - You and your doctor plan to change your medication - You have moderate symptoms and some difficulty with daily functioning **You may NOT be eligible if...** - You are pregnant or breastfeeding - You have previously taken clozapine - You have a known allergy or contraindication to clozapine - You have active suicidal plans or intent - You have severe alcohol or cannabis use disorder, or another active substance use disorder - You are currently in remission (your symptoms are already well-controlled) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGClozapine

Participants are randomized to clozapine or second-line antipsychotics. When randomised to clozapine, they will receive clozapine for six weeks.

DRUGSecond-line Antipsychotics (treatment as usual)

Participants are randomized to clozapine or second-line antipsychotics. When randomized to second-line antipsychotics, this means participants will receive treatment as usual. The physician has the choice to administer any second-line antipsychotic. More specification is not possible, as this is a choice the physician makes with the participant based on the characteristic and preference of the participant (in line with standard clinical practice).


Locations(13)

Medical University Innsbruck

Innsbruck, Austria

Bezirkskliniken Schwaben, Bezirkskrankenhaus Augsburg

Augsburg, Germany

Universitätsklinik für Psychiatrie und Psychotherapie Bielefeld

Bielefeld, Germany

LWL-Klinik Dortmund, Bereich Forschung & Wissenschaft

Dortmund, Germany

University Hospital Frankfurt am Main - Goethe University

Frankfurt am Main, Germany

Klinik für Psychiatrie und Psychotherapie der Universitätsmedizin Mainz

Mainz, Germany

Westfälische Wilhelms-Universität Münster

Münster, Germany

Universita degli Studi di Brescia

Brescia, Italy

University of Cagliari

Cagliari, Italy

Università degli studi della Campania Luigi Vanvitelli

Naples, Italy

Azienda Ospedaliero-Universitaria "Città della Salute e della Scienza di Torino"

Turin, Italy

Fundació Clínic per a la Recerca Biomèdica

Barcelona, Spain

King's College London, Psychiatry & Cognitive Neuroscience

London, United Kingdom

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05958875


Related Trials