Effect of Pharyngeal Inhibition by rTMS on Swallowing Function

NCT ID: NCT02170454

Last Updated: 2014-06-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-06-30

Study Completion Date

2009-06-30

Brief Summary

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The aim of this study is to test the hypothesis that rTMS on the dominant swallowing hemisphere is able to modify swallowing coordination.

Detailed Description

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The aim of the study is to demonstrate that rTMS (on the dominant hemisphere, on the nondominant hemisphere and placebo rTMS) are able to modify swallowing coordination on healthy subjects. Swallowing function will be studied before and after rTMS with videomanometry.

Conditions

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Oropharyngeal Dysphagia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

SINGLE

Participants

Study Groups

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rTMS

rTMS on pharyngeal cortical area in healthy subjects

Group Type ACTIVE_COMPARATOR

magnetic stimulation

Intervention Type PROCEDURE

rTMS on pharyngeal cortical area in healthy subjects or sham rTMS on pharyngeal cortical area in healthy subjects

Placebo

Sham rTMS on pharyngeal cortical area in healthy subjects

Group Type PLACEBO_COMPARATOR

magnetic stimulation

Intervention Type PROCEDURE

rTMS on pharyngeal cortical area in healthy subjects or sham rTMS on pharyngeal cortical area in healthy subjects

Interventions

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magnetic stimulation

rTMS on pharyngeal cortical area in healthy subjects or sham rTMS on pharyngeal cortical area in healthy subjects

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* 18-50 years old
* healthy subjects

Exclusion Criteria

* epilepsia
* brain injury
* stroke
* pregnancy
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Rouen

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Eric VERIN, MDPhD

Role: PRINCIPAL_INVESTIGATOR

Rouen University

Locations

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VERIN

Rouen, , France

Site Status

Countries

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France

Other Identifiers

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2007/055/HP

Identifier Type: -

Identifier Source: org_study_id

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