Treatment Resistance in Psychiatric Disorders: the Search for Biological Markers Predictive of Response to Treatment
- Sponsor
- Centre Hospitalier St Anne
- Study ID
- NCT07741981
- Status
- Not Yet Recruiting
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Conditions
- Bipolar Disorder (BD)
- Catatonia
- Obsessive Compulsive Disorder (OCD)
- Schizophrenia
- Treatment Resistant Depression (TRD)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Blood sampling, lumbar puncture, stool sampling, skin microbiopsy and psychometrics scales — BIOLOGICALthe biomarker research involves different biological sampling : blood, stool, cerebrospinal fluid, skin
Study Details
The disruption of immune system is a key candidate in the pathogenesis of psychiatric disorders, especially those resistant to traditional treatments. Involving complex processes within the brain and peripheral immune system, inflammation may lead to imbalance of neurotransmitter systems and synaptic plasticity and directly contribute to the psychiatric symptoms observed in conditions such as depression, bipolar disorder (BD) and schizophrenia (SCZ). Studies show that treatment-resistant depression (TRD) is associated with elevated levels of inflammatory markers in the blood, which are linked to a lower response to conventional antidepressants. Interventions that modulate this inflammatory response, such as immunomodulatory treatments or therapies targeting pro-inflammatory cytokines, have demonstrated beneficial effects by reducing symptoms and improving patients' quality of life. A thorough understanding of the links between inflammation and treatment resistance therefore paves the way for innovative therapeutic strategies. These approaches could transform current practices by offering more personalized and effective solutions for patients suffering from chronic and resistant psychiatric disorders.
Key Dates
- First listed
- Aug 3, 2026
- Start date
- Jul 15, 2026
- Status verified
- Jun 2026
- Primary completion
- Oct 1, 2036
- Completion
- Aug 1, 2038
Study Design
- Enrollment
- 700 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Other: OCD cohortPatients suffering from OCD resistant to treatments
- Other: Catatonia cohortPatients suffering from resistant catatonia
- Other: TRD cohortPatients suffering from treatment resistant depression (TRD)
- Other: BD cohortPatients suffering from treatment resistant bipolar disorders (BD)
- Other: Schizophrenia cohortPatients suffering from schizophrenia resistant to treatments
Primary Outcome Measure
Changes from inclusion (V1) in disease scale scores at the end of acute phase therapy (V3) [ Time Frame: Up to 10 weeks ]
Central Contacts
- Iolanda PALIMARU, MD+33145658798
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