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.

Status: Recruiting
Location: See all (13) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• In- or out patients, at least 18 years of age up until 70.

• Being willing and able to provide written informed consent. Having a legal guardian to cosign is allowed. Informed consent will be signed at visit 1, before any study procedure.

• Female subjects of child bearing potential must use effective contraception during the trial as per the requirements of the applicable SmPCs and should have a negative pregnancy test at visit 1 or 2 (before randomisation; section 8.2).

• Meeting diagnostic criteria for a primary diagnosis of schizophrenia, schizoaffective disorder, or schizophreniform disorder, according to DSM-5. The primary diagnosis will be confirmed by the Mini International Neuropsychiatric Interview (MINI v7.0.2).

• Subject experiences a treatment failure due to lack of efficacy in the current episode, as confirmed by a CGI-I ≥3; preferably this treatment is a first-line pharmacotherapeutic agent for the primary DSM-5 diagnosis, and was prescribed for at least 4 weeks within an effective dose range as specified in the Summary of Product Characteristics (SmPCs). However, other lines of treatment are accepted as well.

• Subject and clinician intend to change pharmacotherapeutic treatment.

• A minimum symptom severity threshold needs to be present (moderate level; see below) and subject needs to experience functional impairment.

‣ The minimum symptom severity threshold is at least 2 PANSS positive or negative items with a score of 4, or at least one PANSS positive or negative item with a score of 5.

⁃ Functional impairment is defined as a score of 5 or higher on any of the three scales of the Sheehan Disability Scale (SDS).

Locations
Other Locations
Austria
Medical University Innsbruck
RECRUITING
Innsbruck
Germany
Bezirkskliniken Schwaben, Bezirkskrankenhaus Augsburg
NOT_YET_RECRUITING
Augsburg
Universitätsklinik für Psychiatrie und Psychotherapie Bielefeld
RECRUITING
Bielefeld
LWL-Klinik Dortmund, Bereich Forschung & Wissenschaft
RECRUITING
Dortmund
University Hospital Frankfurt am Main - Goethe University
RECRUITING
Frankfurt Am Main
Klinik für Psychiatrie und Psychotherapie der Universitätsmedizin Mainz
RECRUITING
Mainz
Westfälische Wilhelms-Universität Münster
RECRUITING
Münster
Italy
Universita degli Studi di Brescia
RECRUITING
Brescia
University of Cagliari
RECRUITING
Cagliari
Università degli studi della Campania Luigi Vanvitelli
RECRUITING
Naples
Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino
RECRUITING
Turin
Spain
Fundació Clínic per a la Recerca Biomèdica
RECRUITING
Barcelona
United Kingdom
King's College London, Psychiatry & Cognitive Neuroscience
RECRUITING
London
Contact Information
Primary
Inge Winter, Dr.
i.winter@umcutrecht.nl
+31875553227
Backup
Cynthia Okhuijsen-Pfeifer, Dr.
c.pfeifer@umcutrecht.nl
+31875553227
Time Frame
Start Date: 2024-08-01
Estimated Completion Date: 2028-06-30
Participants
Target number of participants: 418
Treatments
Experimental: Schizophrenia early intensified treatment (EIPT): Switch to clozapine
Subject with schizophrenia, randomized to EIPT: Switch to clozapine. Brand, dosage, frequency and duration up to the investigator's discretion
Active_comparator: Schizophrenia treatment as usual (TAU): second-line antispychotic
Subject with schizophrenia or related disorder randomized to TAU: switch to second-line antispychotic. Compound, brand, dosage, frequency and duration up to the investigator's discretion (in accordance with SmPC)
Related Therapeutic Areas
Sponsors
Collaborators: Universität Münster
Leads: Dr. Inge Winter

This content was sourced from clinicaltrials.gov

Similar Clinical Trials