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tDCS Stimulation to Treat Patients With Severe and Resistant Obsessive Compulsive Disorder-Pilot Study

NCT03284671 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2017-09-15

No results posted yet for this study

Summary

The purpose is to show that bifocal tDCS with an anodal stimulation on the orbitofrontal cortex and cathodic stimulation on supplementary motor areas is an effective treatment for patients with resistant and severe obsessive compulsive disorders.

Conditions

  • Obsessive-compulsive Disorders and Symptoms

Interventions

OTHER

bifocal stimulation with tDCS

Patients will receive an active Treatment with tDCS (10 sessions of 30 mn with an intensity of 2 mA)

Sponsors & Collaborators

  • Centre Hospitalier Henri Laborit

    lead OTHER

Principal Investigators

  • Nematollah JAAFARI, Professor · Centre Hospitalier Henri Laborit

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-02-19
Primary Completion
2016-02-19
Completion
2017-05-12

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03284671 on ClinicalTrials.gov