Actively Recruiting

Phase 3
Age: 18Years +
All Genders
NCT05973786

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

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

AI-Powered 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

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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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