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Study identifier: NCT07705802 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Not Yet RecruitingREPSYRE

Outcome of Patients With Severe Mental Illness in the Intensive Care Unit

Condition: Severe Mental Illness · Severe Mental Disorder  ·  Sponsor: Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer

PhaseN/A
Planned participants2000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where30 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

Severe mental illnesses (SMIs), such as major depression, schizophrenia, and bipolar disorder, carry a significant prevalence among patients admitted to the intensive care unit (ICU), estimated at an average of 19%. Evidence indicates that ICU hospitalization is associated with a poorer prognosis regarding mental health and morbi-mortality compared to hospitalization in conventional wards. Despite this recognized vulnerability, available data remain limited and are often derived from retrospective studies with conflicting results. Some studies have shown that SMIs impact neither critical care nor long-term mortality. Conversely, other research has reported higher hospital mortality, an increase in complications (such as mechanical ventilation and prolonged length of stay), and unfavorable functional outcomes. Regarding specific conditions like septic shock, unexpected findings have been observed, with certain SMIs appearing to be associated with reduced 90-day mortality compared to a matched control population. Patients with SMIs thus represent a vulnerable population whose management in the ICU setting may pose specific challenges. This prospective, multicenter study aims to evaluate mortality and identify predictive factors of mortality among patients with SMIs managed in French ICUs.

This description comes directly from the study's public registry record.

Talk to the study team

Magali CESANA, MSc  ·  04 83 77 20 60  ·  magali.cesana@ch-toulon.fr

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Age ≥ 18 years. * Admission to a participating ICU. * Unscheduled ICU admission for medical management, urgent post-operative care, or due to a complication of elective surgery. * Pre-existing diagnosis of a severe mental illness prior to ICU admission, according to DSM-5 criteria: schizophrenia, schizoaffective disorder, severe major depressive episode, chronic depressive disorder, recurrent depressive disorder, or bipolar disorders. * Current chronic treatment with psychotropic medication at the time of enrollment (antidepressants, neuroleptics, other antipsychotics, lithium, or antiepileptic drugs used as mood stabilizers). * Non-opposition to participate from the patient; if the patient is unable to receive information, non-opposition from a relative/trusted person; for patients under guardianship or curatorship, non-opposition from both the legal guardian and the patient. Exclusion Criteria: * Scheduled ICU admission following elective surgery. * Prior enrollment in the REPSYRE study. * Inability to speak or understand French. * Homeless patients or individuals deprived of liberty. * Any other condition or reason that, in the investigator's judgment, might interfere with the evaluation of the study objectives.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (30)

Centre Hospitalier Universitaire de NiceNice, Alpes-Maritimes, France
Groupe Hospitalier Littoral AtlantiqueLa Rochelle, Charente-Maritime, France
Hôpital privé Claude GalienQuincy-sous-Sénart, Essonne, France
CHU Ambroise Paré AP-HPBoulogne-Billancourt, Hauts-de-Seine, France
Centre Hospitalier Universitaire de RennesRennes, Ille-et-Vilaine, France
Centre Hospitalier Simone VeilBlois, Loir-et-Cher, France
Centre Hospitalier de CahorsCahors, Lot, France
Centre Hospitalier Bretagne Atlantique de VannesVannes, Morbihan, France
CHU de Lille - Hôpital Roger SalengroLille, Nord, France
Hôpital Saint Louis (AP-HP)Paris, Paris, France
Hôpital La Pitié SalpêtrièreParis, Paris, France
Hôpital La Pitié SalpêtrièreParis, Paris, France

+ 18 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

NiceLa RochelleQuincy-sous-SénartBoulogne-Billancourt

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