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Repetitive Transcranial Magnetic Stimulation

Not Applicable
Completed
Conditions
Schizophrenia
Interventions
Procedure: rTMS, "repetitive transcranial magnetic stimulation"
Other: rTMS
Registration Number
NCT00169689
Lead Sponsor
Heinrich-Heine University, Duesseldorf
Brief Summary

The study is a prospective, randomized, double-blind sham-controlled study.

Detailed Description

The principal objective of this trial is to investigate the effect of left prefrontal high frequency rTMS on negative symptoms in schizophrenia.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • DSM-IV criteria for schizophrenia
  • age between 18 and 60
  • informed consent
  • right handed patient
  • no change of antipsychotic treatment > 2 weeks before recruitment
Exclusion Criteria
  • seizures, epilepsy
  • history of severe head injury
  • status post implantation of a cardiac pacemaker or other electronic devi-ses

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
rTMSrTMSsham coil system versus verum rTMS stimulation
rTMSrTMS, "repetitive transcranial magnetic stimulation"sham coil system versus verum rTMS stimulation
Primary Outcome Measures
NameTimeMethod
Clinical Global Impression;November 2007
Secondary Outcome Measures
NameTimeMethod
Global psychosocial functioning (GAF), PANSS-Negative Subscale,changes in EEG, heart rate variability, cortisol daytime profile, catecholamines, cognitive functioningNovember 2007

Trial Locations

Locations (1)

Joachim Cordes

🇩🇪

Düsseldorf, Rhineland, Germany

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