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Tests brain stimulation to ease suicidal thoughts in depression

Tests brain stimulation with a mild current in adults with treatment-resistant depression.

Plain-language title generated from the registry record
Registry title: Effects of Transcranial Direct Current Stimulation (tDCS) in the Management of Suicidal Ideation

Key facts

Where
Faye-l'Abbesse and Poitiers, FranceSee the 2 sites

Where in France

  • Centre Hospitalier Nord-Deux-SèvresFaye-l'Abbesse, FranceTaking people
  • Centre Hospitalier Henri LaboritPoitiers, FranceTaking people

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Trial details

Who runs it
Centre Hospitalier Henri Laborit
Trial code
NCT06009523
Record updated
23 October 2026
Original description
The main objective of this study is to demonstrate that 15 transcranial direct current stimulation (tDCS) sessions of 30 minutes at 2 mA intensity are effective to reduce suicidal ideationRead full original descriptionShow less

Effects of Transcranial Direct Current Stimulation (tDCS) in the Management of Suicidal Ideation in Treatment-resistant Depression : a Pilot Study

The main objective of this study is to demonstrate that 15 transcranial direct current stimulation (tDCS) sessions of 30 minutes at 2 mA intensity are effective to reduce suicidal ideation

Inclusion: Age over 18 years; Written informed consent; Diagnosis of recurrent or isolated depressive episode according to DSM IV criteria (A.P.A. 1994); Stable antidepressant treatment for 3 weeks; MADRS score ≥ 20; SSI score > 3; Subject affiliated to a health insurance system; Woman with effective contraception and agreeing to maintain it throughout the study period.

Exclusion: Patient who has already undergone an electroconvulsive therapy course for the current episode and does not respond to this treatment; Contraindication to tDCS: intracerebral metallic implant (with the exception of dental implants), cardiac pacemaker, active or non-implanted devices in the region of the head, acute eczema in the planned stimulation area; Depression with psychotic features Axis I (DSM IV) co-morbid diagnosis of schizophrenia, alcohol and/or other substance dependence (or abuse) (lifetime); Patient deprived of liberty; Patient with high suicide risk (item 10 MADRS > 4) in the absence of hospitalization; Pregnant, parturient or breastfeeding woman; Simultaneous participation in another interventional research.

ClinicalTrials.gov NCT06009523