Actively Recruiting
The Effect of a Six Week Intensified Pharmacological Treatment for Bipolar Depression Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment.
Led by Dr. Inge Winter · Updated on 2025-09-26
418
Participants Needed
13
Research Sites
176 weeks
Total Duration
On this page
Sponsors
D
Dr. Inge Winter
Lead Sponsor
U
Universität Münster
Collaborating Sponsor
AI-Summary
What this Trial Is About
Bipolar disorders affect approximately 4.5 million people across the European Union (EU) and are associated with high annual healthcare and societal costs. Bipolar disorder I and II represent disorders that cause extreme fluctuation in a person's mood, energy, and ability to function, in which symptoms of (hypo)mania and depression alternate. The depressive episodes of bipolar disorders are often referred to as bipolar depression (BD). In other words: it is a phase/state of the disorder. For many patients with BD, the depressive polarity is often more pervasive and more debilitating than manic states, with estimates that depressed mood accounts for up to two-thirds of the time spent unwell, even with treatment. The burden of not received an effective treatment for BD is high: more severe psychopathology, higher rates of unemployment, more hospitalisations, lower quality of life, lower cognitive functioning, risk of suicide, comorbidities and poorer social and occupational functioning and thus more carer burden. For BD, the treatment guidelines are very heterogeneous, amongst other reasons because the disease is heterogeneous and treatments should be tailored to the patients. There is no clear treatment algorithm and it cannot yet be predicted which treatment will be effective. Especially the place of adjunctive antidepressants is under debate. Usually, for psychiatric disorders (including bipolar disorder), a patient is considered to be treatment-resistant is two medicinal treatments have been tried (in sufficient duration and dosage) without sufficient success. For BD, there is no consensus on when to consider a patient as treatment-resistant, but the most common definition is after one prior treatment failure. This raises the research question whether adjunctive antidepressants to treat BD should be introduced earlier in the treatment. Additionally, The INTENSIFY trial is part of the larger Horizon 2021 project, 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, we 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.
CONDITIONS
Official Title
The Effect of a Six Week Intensified Pharmacological Treatment for Bipolar Depression Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be an in- or outpatient aged 18 years or older
- Willing and able to provide written informed consent (legal guardian allowed to cosign)
- Female participants of childbearing potential must use effective contraception and have a negative pregnancy test before randomization; male participants using valproate acid must use effective contraception
- Diagnosed with bipolar depression type I or II currently in a depressive episode confirmed by MINI v7.0.2
- Experienced treatment failure due to lack of efficacy on current episode, preferably first-line treatment prescribed for at least 4 weeks at effective dose
- Both participant and clinician intend to change pharmacological treatment
- Have moderate symptom severity (MADRS score ≥ 20) and functional impairment (score ≥ 5 on any Sheehan Disability Scale domain)
You will not qualify if you...
- Being pregnant or breastfeeding
- Known intolerance to quetiapine or any study medications for either treatment arm
- Any contraindications to study medications supported by abnormal lab tests, ECG, or physical exam
- Participation in another clinical trial with investigational drug within 30 days before screening
- Any other significant disease or disorder that increases risk or affects trial participation or results
- Active suicidal ideation with intent or plan as assessed by C-SSRS and clinician judgment
- Current substance use disorder except nicotine dependency and mild/moderate alcohol or cannabis use disorder
- Legal commitment to an institution by judicial or administrative order
- Young Mania Rating Scale score of 12 or higher indicating predominant manic or mixed symptoms
- Dependence on sponsor, investigator, or trial site
- Pre-existing severe liver damage
- History of antidepressant-induced mania/hypomania or recent rapid cycling
AI-Screening
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Trial Site Locations
Total: 13 locations
1
Medical University Innsbruck
Innsbruck, Austria
Actively Recruiting
2
Universitätsklinik für Psychiatrie und Psychotherapie Bielefeld
Bielefeld, Germany
Actively Recruiting
3
LWL-Klinik Dortmund, Bereich Forschung & Wissenschaft
Dortmund, Germany, 44287
Actively Recruiting
4
University Hospital Frankfurt am Main - Goethe University
Frankfurt am Main, Germany
Actively Recruiting
5
Klinik für Psychiatrie und Psychotherapie der Universitätsmedizin Mainz
Mainz, Germany
Actively Recruiting
6
Westfälische Wilhelms-Universität Münster
Münster, Germany
Actively Recruiting
7
Eginition hospital, department of psychiatry
Athens, Greece, 11528
Not Yet Recruiting
8
Universita degli Studi di Brescia
Brescia, Italy
Actively Recruiting
9
University of Cagliari
Cagliari, Italy
Actively Recruiting
10
Università degli studi della Campania Luigi Vanvitelli
Naples, Italy, 80138
Actively Recruiting
11
Azienda Ospedaliero-Universitaria "Città della Salute e della Scienza di Torino"
Turin, Italy
Actively Recruiting
12
Fundació Clínic per a la Recerca Biomèdica
Barcelona, Spain
Actively Recruiting
13
King's College London, Psychiatry & Cognitive Neuroscience
London, United Kingdom, SE5 8AF
Not Yet Recruiting
Research Team
I
Inge Winter, Dr.
CONTACT
C
Cynthia Okhuijsen-Pfeifer, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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