Status:

COMPLETED

Study of Morphological and Perfusion Imaging Predictors of Pejorative Outcome in Major Depressive Disorder

Lead Sponsor:

Rennes University Hospital

Conditions:

Depressive Disorder

Eligibility:

All Genders

18+ years

Brief Summary

Depression is a debilitating illness with a risk of developing a treatment resistant form. Currently, diagnosis is purely clinical with little features available to identify potentially adverse develo...

Detailed Description

The main objective is to assess neuroimaging biomarkers like cortical thickness predictive of poor outcome in major depressive disorder. Secondary objectives are : * Identifying neuroimaging biomark...

Eligibility Criteria

Inclusion

  • Men and women aged over 18 years;
  • Patient with a diagnosis (according to DSM IV criteria measured at MINI) for Major Depressive Episode, and / or recurrent depressive disorder unipolar or bipolar , or chronic and resistant depression (according to the criteria of Thase and Rush);
  • Patients will be stratified as the stages of classification and Thase Rush scale widely used to characterize the therapeutic resistance in depression;
  • Intensity of EDM with a minimum score of 15 (MADRS);
  • Patient in receiving information on the protocol;
  • Patient who received information about the protocol and did not express opposition to participate.

Exclusion

  • Related to MRI
  • Pacemaker or implantable defibrillator;
  • Neurosurgical clips;
  • Cochlear implants;
  • Metal intra orbital or encephalic foreign bodies;
  • Stents placed for less than four weeks and osteosynthesis material posed for less than six weeks;
  • Claustrophobia.
  • Other criteria
  • Pregnant or lactating women;
  • Hemodynamically unstable acute respiratory failure , a general poor condition or a need for monitoring incompatible with the constraints of MRI ;
  • Legal protection ;
  • Patients hospitalized without their consent.

Key Trial Info

Start Date :

November 3 2014

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

August 5 2021

Estimated Enrollment :

179 Patients enrolled

Trial Details

Trial ID

NCT02286024

Start Date

November 3 2014

End Date

August 5 2021

Last Update

February 13 2023

Active Locations (1)

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1

Centre Hospitalier Guillaume Regnier

Rennes, Britanny, France, 35000