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Clinical Trials/NCT04354935
NCT04354935
Recruiting
Not Applicable

Treatment of Resistant Depression by Repetitive Transcranial Magnetic Stimulation (rTMS) Multicentric Naturalistic Study

Centre hospitalier de Ville-Evrard, France2 sites in 1 country160 target enrollmentOctober 18, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
To Evaluate the Effectiveness of Open rTMS
Sponsor
Centre hospitalier de Ville-Evrard, France
Enrollment
160
Locations
2
Primary Endpoint
measure the evolution of the HDRS-17 score
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Repetitive Transcranial Magnetic Stimulation (rTMS) for repetitive Transcranial Magnetic Stimulation) is a a recent technique to stimulate the brain in a way that non-invasive, for therapeutic purposes. The first trials of analgesic use of rTMS date back to about 15 years ago. years and clinical use has now entered the practice of some specialized centers. Used at a frequency less than or equal to 1 Hertz (Hz; a stimulation per second), it is called bass rTMS. frequency and results in inhibition of cortical excitability at the level of the stimulated area. Conversely, a stimulation with a frequency higher than 5 Hz, called high-frequency rTMS, will have an excitatory effect on the targeted neurons. In addition to its local effects at the stimulation site, rTMS can also have effects on distance on regions other than those directly targeted. The impact of this treatment would be the local modulation of the cerebral plasticity and also act on the anatomical connectivity and functional brain function in both healthy subjects and those who are patients with psychiatric disorders

Detailed Description

Main objective : To show the effectiveness of rTMS carried out in open on the symptoms of depression resistant in common practice between the Baseline and the end of the initial treatment (between 1 and 6 weeks). Secondary Objectives Evaluate the tolerance of the rTMS carried out in open on the symptoms of depression resistant in common practice between the Baseline and the end of the initial cure (between 1 and 6 weeks) Evaluate the impact of this treatment on : * The response rate * The remission rate * Quality of life To assess the correlation between personality dimensions and depression. The criteria main evaluation : The evolution of the HDRS-17 score (Hamilton depression scale, 17 items) between the Baseline and the end of the initial treatment (1 to 6 weeks) The evaluation criteria secondary : * Responder patient rate (defined as a 50% decrease in the rate of % of HDRS score) * Rate of patients in remission (defined by HDRS score\<8) * Evolution of the EQ5D quality of life score between Baseline and end of the initial treatment (between 1 and 6 weeks)

Registry
clinicaltrials.gov
Start Date
October 18, 2019
End Date
February 28, 2026
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Centre hospitalier de Ville-Evrard, France
Responsible Party
Principal Investigator
Principal Investigator

Noomane Bouaziz, MD

psychiatrist

Centre hospitalier de Ville-Evrard, France

Eligibility Criteria

Inclusion Criteria

  • Presenting a depressive episode characterized as resistant according to the DSM 5 criteria
  • resistance is characterized by: non-response to at least two different antidepressants prescribed at effective doses for a duration greater than or equal to 6 weeks.
  • Patient who agrees to participate in the study and who has signed an informed consent.
  • Patient fluent in French
  • Affiliation to a social security scheme.
  • Women of childbearing age must be on contraception

Exclusion Criteria

  • Presenting a contraindication to TMS: intrafemale foreign body cranial, unstable epilepsy, cochlear implant, pacemaker, pregnancy
  • Presence of a psychotic disorder
  • Presence of an unstable medical condition
  • Presence of schizophrenia or persistent delusional disorder
  • Persons under guardianship, curatorship and safeguarding of justice.
  • Pregnant women,
  • Woman of childbearing age without effective contraception
  • Breastfeeding woman

Outcomes

Primary Outcomes

measure the evolution of the HDRS-17 score

Time Frame: an average of 1 year

The evolution of the HDRS-17 score (Hamilton depression scale, 17 items) between the Baseline and the end of the initial 4 to 6 week treatment course

Secondary Outcomes

  • Rate of responding patients(an average of 1 year)
  • Evolution of the quality of life score(an average of 1 year)
  • Rate of patients in remission(an average of 1 year)

Study Sites (2)

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