ClinicalTrials.Veeva

Menu

Biocollection on Peripheral Inflammation (IBIS-PSY)

N

Nantes University Hospital (NUH)

Status

Enrolling

Conditions

Bipolar Disorder I
Bipolar Disorder II
Schizoaffective Disorder, Depressive Type

Treatments

Biological: Peripheral venipuncture blood sampling, as part of standard care procedures
Other: Interview with a psychiatrist

Study type

Observational

Funder types

Other

Identifiers

NCT05934474
RC23_0270

Details and patient eligibility

About

Most psychiatric research is based on the nosographic classifications used in current practice. At present, there is no diagnostic or prognostic biomarker for psychiatric pathologies commonly used in clinical practice. The study hypothesis is that peripheral inflammatory biomarkers could be common to several psychiatric disorders, in particular psychotic disorders (bipolar disorder, schizophreniform disorder, schizophrenia, depressive episode with psychotic features). The aim of this project is to set up a bio-collection of biological samples (peripheral blood samples) with associated phenotypic data (assessment of various symptoms using standardized scales in patients whose blood is sampled). The setting up of this cohort follows on from work carried out on a PsyCourse cohort also using a transdiagnostic approach in psychiatry, in order to be able to collaborate within a European research project.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Major patient

  • Patient with one of the following diagnoses confirmed by a psychiatrist:

    • Characterized depressive episode with psychotic features,
    • Bipolar disorder type I
    • Bipolar disorder type II
    • Schizoaffective disorder
    • Schizophrenia
    • Schizophreniform disorder
  • Patient under psychiatric care at Nantes University Hospital

  • Patients weighing at least 45kg

  • Patient affiliated to a social security scheme or beneficiary of such a scheme

  • Patient who has given informed consent to participate in the study

Exclusion criteria

  • Pregnant,
  • History of cancer in the last 5 years,
  • Vaccination within the last 4 weeks,
  • Acute or chronic infection,
  • Medical history of organ transplant,
  • Medical history of autoimmune disease,
  • Hearing impairment making it impossible to complete study questionnaires,
  • Patient under court protection

Trial design

300 participants in 1 patient group

IBIS-PSY patients
Treatment:
Biological: Peripheral venipuncture blood sampling, as part of standard care procedures
Other: Interview with a psychiatrist

Trial contacts and locations

1

Loading...

Central trial contact

Anne Sauvaget

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems