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Repetitive Transcranial Stimulation (rTMS) in Post Stroke Dysphagia

Phase 4
Completed
Conditions
Dysphagia
Stroke
Interventions
Device: rTMS
Device: Placebo rTMS
Registration Number
NCT01081444
Lead Sponsor
University Hospital, Rouen
Brief Summary

The aim of this study is to assess if rTMS on healthy hemisphere at one hertz could improve patients with post stroke dysphagia.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • dysphagia
  • first episode of stroke
Exclusion Criteria
  • swallowing disorder before stroke
  • previous episode of stroke
  • MMS < 20 no consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1rTMSActive rTMS
2Placebo rTMSsham rTMS
Primary Outcome Measures
NameTimeMethod
Videofluoroscopy and high resolution manometryday 0, day 14, day 30, day45
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Physiology, Rouen University Hospital

🇫🇷

Rouen, France

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