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PROSPECTIVE EVALUATION OF BLOOD BIOMARKERS AS AN AID TO DIAGNOSTIC AND TREATMENT IN DRUG-NAIVE PATIENTS WITH DEPRESSION

EVALUATION PROSPECTIVE DE L'AIDE AU DIAGNOSTIC ET AU TRAITEMENT PAR BIOMARQUEURS SANGUINS CHEZ DES PATIENTS DRUG-NAÏFS AMBULATOIRES SOUFFRANT DE DEPRESSION

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06369792
Enrollment
200
Registered
2024-04-17
Start date
2020-10-20
Completion date
2024-12-31
Last updated
2024-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bipolar Depression, Bipolar Disorder, Depressive Disorder

Brief summary

This is an observational (non-interventional) prospective study, carried out in drug-naïve outpatients who start a treatment with escitalopram, fluoxetine, sertraline or quetiapine. Five blood samples are collected (i.e. before initiating the drug, and then after 1, 2, 4 and 8 weeks of treatment). It does not affect the choice or the treatment dose. The primary objective of this study is to measure the association between the EDIT-B® editing signature and response to pharmacological treatment in drug-naïve patients. Results of this research could provide an aid to early diagnosis, optimize pharmacological treatment and guide clinical practice towards individualized treatment.

Interventions

None listed

Sponsors

Les Toises - Psychiatry and Psychotherapy Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult drug-naïve outpatients suffering from depression and/or bipolar disorders who start a pharmacological treatment with escitalopram, fluoxetine, sertraline or quetiapine and who gave his written informed consent to participate in the present study.

Exclusion criteria

* Any patient without capacity of discernment or with harmful use of psychoactive substances

Design outcomes

Primary

MeasureTime frameDescription
psychiatric symptomatologyAt baseline, 1,2,4,8 weeksself- and hetero-questionnaire psychiatric scales
EDIT-B profilingAt baseline, 1,2,4,8 weeksMeasurement of RNA editing over time

Countries

Switzerland

Contacts

Primary ContactAurélie Reymond-Delacrétaz, PhD
aurelie.delacretaz@lestoises.ch0041 584-580-580

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026