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Clinical Trials/NCT01132066
NCT01132066
Completed
Phase 1

Pilot Study of Transcranial Direct Current Stimulation for Facilitating Swallowing Improvement After an Acute Unilateral Hemispheric Infarction

Beth Israel Deaconess Medical Center1 site in 1 country19 target enrollmentApril 2007
ConditionsDysphagia

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Dysphagia
Sponsor
Beth Israel Deaconess Medical Center
Enrollment
19
Locations
1
Primary Endpoint
Dysphagia Outcome and Severity Scale Score (DOSS)
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The purpose of the research study is to investigate the effect of a brain stimulation technique called Transcranial Direct Current Stimulation (TDCS) in improving swallowing functions in subjects who develop dysphagia after a unilateral hemispheric infarction.

Registry
clinicaltrials.gov
Start Date
April 2007
End Date
May 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sandeep Kumar

Assistant Professor of Neurology

Beth Israel Deaconess Medical Center

Eligibility Criteria

Inclusion Criteria

  • Acute ischemic stroke
  • Between 24-168 hours after onset
  • Moderate to severe dysphagia based on swallowing assessment

Exclusion Criteria

  • Preexisting swallowing impairment
  • Intracerebral hemorrhage
  • Pacemaker of other electrically sensitive device

Outcomes

Primary Outcomes

Dysphagia Outcome and Severity Scale Score (DOSS)

Time Frame: 5 days after study enrollment

DOSS is a validated swallowing assessment scoring system that will rate the severity of dysphagia. It will be performed by a speech and swallow pathologist.

Secondary Outcomes

  • Incidence of seizure(5 days after study enrollment)

Study Sites (1)

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