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Effect of Transcranial Direct Current Stimulation (tDCS) on the Excitability of the Diaphragmatic Primary Motor Cortex

I

Institut National de la Santé Et de la Recherche Médicale, France

Status

Completed

Conditions

Excitability of Diaphragmatic Primary Motor Cortex

Treatments

Device: Eldith DC stimulator ( Magstim Company Ltd. UK)

Study type

Interventional

Funder types

Other

Identifiers

NCT01548586
C10-52
2011-A00508-33 (Registry Identifier)

Details and patient eligibility

About

Transcranial direct current stimulation (tDCS) is a non invasive, painless, harmless way to modulate cerebral cortex excitability. It was shown that anodal stimulation increases cortical excitability and the cathodal one decreases it (Nitsche and Paulus, 2000; Lang et al. 2004). To date, there is no data in the literature regarding the effect of tDCS on the corticodiaphragmatic pathways. This preliminary study aims to test and validate the modulating effect of tDCS on the excitability of the primary motor cortex dedicated to the hemi-diaphragms in a sample of healthy subjects, as a prelude to further large studies in patients with paretic hemi-diaphragms. Diaphragmatic motor evoked potentials will be assessed before and after applications of three different modalities of tDCS (anodal, cathodal and placebo).

Full description

We therefore expect to observe a significant increase of the mean values of the right hemidiaphragm's MEP's amplitudes after application of anodal tDCS compared to the baseline MEP obtained before this treatment.

Enrollment

12 patients

Sex

Male

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Right handed,
  • Healthy male volunteers
  • Aged ≥ 18 and ≤ 35 years
  • No history of neurological or respiratory disease
  • BMI (body mass index < 30)

Exclusion criteria

  • Female sex
  • Vulnerable people as defined in the provisions relating to biomedical researches and described in the Code of Public Health.
  • Recent or ongoing use of antibiotic drugs, antidepressants or psychotropic drugs.
  • Recent hospitalization (within 3 months).
  • No affiliation to a social security system.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

12 participants in 3 patient groups, including a placebo group

Anodal tDCS
Active Comparator group
Treatment:
Device: Eldith DC stimulator ( Magstim Company Ltd. UK)
Cathodal tDCS
Active Comparator group
Treatment:
Device: Eldith DC stimulator ( Magstim Company Ltd. UK)
Placebo type tDCS
Placebo Comparator group
Treatment:
Device: Eldith DC stimulator ( Magstim Company Ltd. UK)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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