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Clinical Trial Summary

The purpose of this study is to determine whether tDCS is effective as an add-on treatment in SSRI-resistant patients with obsessive and compulsive disorder


Clinical Trial Description

Total number of scheduled patients to be recruited: 46 We used the effect size of the study of Ruffini and colleagues (2009) in which rTMS was used to target the left orbito frontal cortex to calculate the number of patients to be recruited. With a risk alpha of 5%, a power of 80%, the number of patients to be included was 46 with an anticipated rate of 10% of lost to follow-up patients. (calculation was made on the http://www.spc.univ-lyon1.fr/mfcalc/NSN/assistant.htm)

Statistical analysis to address the primary and secondary objectives:

Chi squared test will be applied for quantitative data. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02407288
Study type Interventional
Source Hôpital le Vinatier
Contact Bation Remy, MD
Phone 33437915565
Email remy.bation@chu-lyon.fr
Status Recruiting
Phase N/A
Start date March 12, 2015
Completion date June 2018

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