Classic vs Deep rTMS for Treatment-Resistant Depression

Effects of a Classic High-frequency rTMS Treatment Versus a Deep rTMS Treatment

Recruiting N/A Interventional Study
Depressive Disorder, Treatment-Resistant
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
152 (estimated)
Sponsor
Centre Hospitalier Henri Laborit · Other
Who this trial is looking for

This trial is looking for adults with treatment-resistant depression to compare two types of brain stimulation treatments. Participants will receive either classic or deep rTMS treatment along with standard therapy, with a total of 20 sessions planned over several weeks.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am over 18 years old
  • I have signed a consent form
  • I have been diagnosed with depressive disorder
  • I have not changed my antidepressant treatment in 3 weeks
  • I have a MADRS score of 21 or higher
  • I am affiliated with a social security regimen

You may not be able to join if

  • I have depression with psychotic features
  • I have had schizophrenia or a substance abuse problem
  • I have already received seismotherapy for my current depression
  • I am under hospitalization or legal protection
  • I am at high risk of suicide without hospitalization
  • I have a personal history of seizures or serious neurological issues
  • I am pregnant
  • I am participating in another intervention study

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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About This Trial
The main objective is to demonstrate that dTMS is more efficient than high frequency rTMS with a conventional coil. The patient will receive treatment arm A or B : Arm A : classic rTMS treatment (use of the 8-shaped coil) and standard therapy Arm B: treatment with deep rTMS (use of the H-shaped coil (helmet)) and standard therapies. 20 rTMS sessions are planned (5 sessions per week) and 3 follo…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Volunteer subjects over 18 years old * Having signed a free and informed consent * Having a diagnostic of caracterised depressive episod recurrent or isolated according to DSM IV criteria (A.P.A 1994). * Having an antidepressant treatment not modified since 3 weeks * Score to …
Contacts

Ghina HARIKA-GERMANEAU, Dr

0033 5 16 52 61 18

ghina.harika-germaneau@ch-poitiers.fr

CONTACT