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Completed

NCT Number: NCT01081444

Repetitive Transcranial Stimulation (rTMS) 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.

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Key information

Conditions

Dysphagia Brain Diseases Cardiovascular Diseases Central Nervous System Diseases Cerebrovascular Disorders Deglutition Disorders Digestive System Diseases Esophageal Diseases Gastrointestinal Diseases Nervous System Diseases Otorhinolaryngologic Diseases Pharyngeal Diseases Stroke Vascular Diseases

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Physiology, Rouen University Hospital

Rouen, 76031, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • dysphagia
  • first episode of stroke

Exclusion criteria

  • swallowing disorder before stroke
  • previous episode of stroke
  • MMS < 20 no consent

Treatment and study plan

rTMS

Device

effective and active cortical magnetic stimulations

placebo rTMS

Device

non active cortical magnetic stimulation

Primary outcomes

  1. Videofluoroscopy and high resolution manometry

    Time frame: day 0, day 14, day 30, day45

Sponsors and collaborators

Lead sponsor

University Hospital, Rouen

Other

Registry information

Official study title

Effect of Pharyngeal Inhibition Induced by Repetitive Transcranial Stimulation in Post Stroke Dysphagia

Acronym: rTMS AVC

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Mar 5, 2010
Registry last updated
Mar 23, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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