Optimize and Predict Antidepressant Efficacy for Patient With MDD Using Multi-omics Analysis and AI-predictive Tool

NCT06550037 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2026-05-15

No results posted yet for this study

Summary

OPADE is a non-profit, observational, multicenter, open-label study aimed at defining personalized treatment for Major Depressive Disorder (MDD). In particular, we will combine genetics, epigenetics, microbiome, immune response data together with anamnesis, questionnaires, electroencephalography (EEG) collected from subjects suffering MDD. Eventually, an Artificial Intelligence (AI)/Machine Learning (ML) predictive tool will be created to guide clinicians in improving MDD treatment and patient's stratification.

Conditions

Sponsors & Collaborators

  • University of Siena

    collaborator OTHER
  • Fundació Eurecat

    collaborator OTHER
  • Perseus Biomics

    collaborator UNKNOWN
  • ARTIFICIAL INTELLIGENCE EXPERT SRL

    collaborator INDUSTRY
  • Mama Health Technologies GmbH

    collaborator INDUSTRY
  • Protobios OU

    collaborator UNKNOWN
  • Cephalgo

    collaborator INDUSTRY
  • Biokeralty Research Institute

    collaborator INDUSTRY
  • Sanitas University

    collaborator OTHER
  • Accare

    collaborator OTHER
  • Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta

    collaborator OTHER
  • Istanbul Medipol University Hospital

    collaborator OTHER
  • CEINGE

    collaborator UNKNOWN
  • Fondazione di ricerca biomedica EBRIS

    collaborator UNKNOWN
  • Alessio Fasano

    lead OTHER

Eligibility

Min Age
14 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-07
Primary Completion
2027-04-30
Completion
2027-05-31

Countries

  • Italy

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06550037 on ClinicalTrials.gov