Cortical Neuromodulation in Post Stroke Dysphagia

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
University Hospital, Rouen
ClinicalTrials.gov Identifier:
NCT01345890
First received: February 17, 2009
Last updated: June 17, 2013
Last verified: June 2013

February 17, 2009
June 17, 2013
January 2007
June 2008   (final data collection date for primary outcome measure)
videofluoroscopy [ Time Frame: before and after (once a day for 5 consecutive days) ] [ Designated as safety issue: No ]
measure swallowing time before and after electrical stimulation, performed one hour per day, 5 consecutive days during paste consistency swallowing
Same as current
Complete list of historical versions of study NCT01345890 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Cortical Neuromodulation in Post Stroke Dysphagia
Neuromodulation in Post Stroke Dysphagia

The investigators aim is to try to rehabilitate post stroke dysphagia using electrical stimulation of the mylohyoid muscles.

Aspiration could have fatal complication especially in post stroke dysphagia. The aim of this study is to improve post stroke dysphagia using electrical stimulation of mylohyoid muscles.

The investigators measure swallowing time before and after electrical stimulation, performed one hour per day, 5 consecutive days during paste consistency swallowing

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Supportive Care
Dysphagia
Procedure: electrical stimulation
sub motor threshold stimulation of mylohyoid muscles
Experimental: electrical stimulation
stroke patients
Intervention: Procedure: electrical stimulation
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
20
June 2010
June 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • post stroke dysphagia

Exclusion Criteria:

  • contraindication to magnetic stimulation, unability to accept the study
Both
18 Years to 80 Years
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT01345890
2004/008/HP
No
University Hospital, Rouen
University Hospital, Rouen
Not Provided
Principal Investigator: Eric VERIN, MD-PhD Rouen University
University Hospital, Rouen
June 2013

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