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Deep Phenotyping for Clinical Inferring Response in Treatment Resistant Depression

Recruitingn/aAges 18 Years - anyAllMax-Planck-Institute of Psychiatry
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In plain words

What the trial is, and whether it could suit you

DECIDE- Deep phenotyping for clinical inferring response in treatment resistant depression -Study Building upon the "Biobanking" initiative at the Max Planck Institute of Psychiatry, the present project aims to identify clinically relevant subtypes of treatment-resistant depression (TRD) through Clinical Deep Phenotyping (CDP). According to clinical trials, 30-40% of the patients suffering from TRD benefit from lithium treatment. By collecting multimodal biological and clinical-diagnostic markers, such as structural and functional brain imaging via magnetic resonance imaging (MRI), brain signals from electroencephalography, comprehensive blood tests, assessment of perception and cognition through neuropsychological testing, as well as the evaluation of specific depression symptoms and psychological and other comorbidities using standardized questionnaires, a bio-clinical signature will

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๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Obligated Participation in "Biobanking" of Max Planck Institute of psychiatry * Age: โ‰ฅ18 years * DSM-V diagnosis of major depressive disorder (MDD; confirmed by Mini-Interview) * Treatment resistant depression (TRD): TRD stage I or TRD stage II * Indication for antidepressant pharmacotherapy * Indication for lithium augmentation * Ability to provide informed consent Exclusion Criteria: * Age: \< 18 years * Medical conditions incompatible with lithium therapy * History of hypomanic or manic episode * Two or more antidepressant substances simultaneously to lithium, except the combination with sleep-promoting antidepressants like Mirtazapine, Mianserin, or Trazodone * An alternative pharmacological augmentation strategy simultaneously to lithium disorder * Quetiapine immediate- and extended release more than 100 mg in total * Current substance use disorder except for moderate alcohol or benzodiazepine use bound to the current episode, or smoking * Patients who are not suitable for the study in the opinion of the investigator * Patients with a relevant comorbidity of the central nervous system such as focal neurological disease (stroke, tumour), current or past epilepsy, CNS inflammation including autoimmune disease, traumatic brain injury, past brain surgery * Patients that are not able to provide informed consent * Electroconvulsive therapy (ECT) in the current depressive episode * Repetitive transcranial magnetic stimulation (rTMS) in the current depressive episode
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What it tests

  • Not listed
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Where

1 site
Max Planck Insitute of Psychiatry
Munich, Germany
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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