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Transcranial Direct Current Stimulation for Dysphagia Therapy in Acute Stroke Patients

U

University Hospital Muenster

Status

Completed

Conditions

Dysphagia
Stroke

Treatments

Device: Sham stimulation
Device: Transcranial direct current stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT01970384
2010-140

Details and patient eligibility

About

The purpose of this study is to evaluate whether transcranial direct current stimulation of the cerebral swallow motor cortex in addition to standard care can enhance recovery of swallow function in acute dysphagic stroke patients compared to sham treatment plus standard care.

Enrollment

60 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • dysphagia due to acute stroke

Exclusion criteria

  • preexisting dysphagia
  • comorbidities that can possibly cause dysphagia
  • psychiatric comorbidities
  • pacemaker or other implanted electronic devices
  • inability to give informed consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 2 patient groups

Transcranial direct current stimulation
Experimental group
Description:
20 Minutes of transcranial direct current stimulation (20 min, 1 mA) administered over the contralesional cortical swallow motor area once daily over 4 consecutive days. In case of a brainstem stroke stimulation will be applied over the cortical swallow motor area of the right hemisphere.
Treatment:
Device: Transcranial direct current stimulation
Sham stimulation
Sham Comparator group
Description:
20 Minutes of sham transcranial direct current stimulation (20 min, no current applied) administered over the contralesional cortical swallow motor area once daily over 4 consecutive days. In case of a brainstem stroke sham stimulation will be applied over the cortical swallow motor area of the right hemisphere.
Treatment:
Device: Sham stimulation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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