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The Effects of TMS on Memory-consolidation in Human Primary Visual Cortex

This study has been withdrawn prior to enrollment.
(Due to administrative issues, the study was withdrawn.)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00480012
First Posted: May 30, 2007
Last Update Posted: August 30, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Sheba Medical Center
  Purpose
Rapid Transcranial Magnetic Stimulation will be used in order to examine whether the human primary visual cortex is essential to visual memory consolidation.

Condition Intervention
Healthy Device: rTMS

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Basic Science
Official Title: The Effects of Transcranial Magnetic Stimulation of the Brain on Memory-consolidation in Human Primary Visual Cortex

Resource links provided by NLM:


Further study details as provided by Sheba Medical Center:

Estimated Enrollment: 0
Study Start Date: May 2005
Estimated Primary Completion Date: June 2007 (Final data collection date for primary outcome measure)
Intervention Details:
    Device: rTMS
    repetitive transcranial meagnetic stimulation of the brain
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy
  • Right handed

Exclusion Criteria:

  • Active/past neurological/psychiatric disorder
  • Personal/first-degree history of seizures
  • Cardio-vascular disorder or disease including hypertension chronic use of medication
  • Metal/electronic device implant
  • Pregnancy
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00480012


Sponsors and Collaborators
Sheba Medical Center
Investigators
Principal Investigator: Revital Amiaz, MD Sheba Medical Center
  More Information

Responsible Party: Amiaz Revital, MD - Senior Psychiatrist, Sheba Medical Center
ClinicalTrials.gov Identifier: NCT00480012     History of Changes
Other Study ID Numbers: SHEBA-04-3437-RA-CTIL
First Submitted: May 29, 2007
First Posted: May 30, 2007
Last Update Posted: August 30, 2011
Last Verified: August 2011

Keywords provided by Sheba Medical Center:
healthy subjects