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Repetitive Transcranial Stimulation (rTMS) in Post Stroke Dysphagia (rTMS AVC)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01081444
First Posted: March 5, 2010
Last Update Posted: March 23, 2012
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 (Responsible Party):
University Hospital, Rouen
August 14, 2009
March 5, 2010
March 23, 2012
March 2009
April 2011   (Final data collection date for primary outcome measure)
Videofluoroscopy and high resolution manometry [ Time Frame: day 0, day 14, day 30, day45 ]
Same as current
Complete list of historical versions of study NCT01081444 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Repetitive Transcranial Stimulation (rTMS) in Post Stroke Dysphagia
Effect of Pharyngeal Inhibition Induced by Repetitive Transcranial Stimulation in Post Stroke Dysphagia
The aim of this study is to assess if rTMS on healthy hemisphere at one hertz could improve patients with post stroke dysphagia.
Not Provided
Interventional
Phase 4
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
  • Dysphagia
  • Stroke
  • Device: rTMS
    effective and active cortical magnetic stimulations
  • Device: Placebo rTMS
    non active cortical magnetic stimulation
  • Active Comparator: 1
    Active rTMS
    Intervention: Device: rTMS
  • Placebo Comparator: 2
    sham rTMS
    Intervention: Device: Placebo rTMS
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
30
October 2011
April 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • dysphagia
  • first episode of stroke

Exclusion Criteria:

  • swallowing disorder before stroke
  • previous episode of stroke
  • MMS < 20 no consent
Sexes Eligible for Study: All
18 Years to 75 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
France
 
 
NCT01081444
2007/122/HP
No
Not Provided
Not Provided
University Hospital, Rouen
University Hospital, Rouen
Not Provided
Principal Investigator: Eric VERIN, MD-PhD Rouen University Hospital
University Hospital, Rouen
March 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP