Skip to main content
Clinical Trials/ISRCTN97286108
ISRCTN97286108
Completed
Not Applicable

Randomised controlled dose response trial of transcranial direct current stimulation for dysphagia after acute stroke

niversity of Manchester0 sites45 target enrollmentApril 2, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity of Manchester
Enrollment
45
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 2, 2015
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Manchester

Eligibility Criteria

Inclusion Criteria

  • 1\. All patients with dysphagia following acute anterior or posterior cerebral circulation stroke that present dysphagia for the first time, within the first weeks from symptoms and up to 6 weeks post stroke. The presence of dysphagia will be based on the results of screening procedures by the research team. Patients will be always recruited after 48\-72 hours post lesion
  • 2\. There is no age limit
  • 3\. Patients must be medically stable
  • 4\. Lesions have to be verified on imaging techniques, either magnetic resonance (MR) scan or computerised tomography (CT), information which will be collected

Exclusion Criteria

  • 1\. Advanced dementia
  • 2\. Other neurological conditions that may explain swallowing difficulty (dysphagia)
  • 3\. Previous history of dysphagia
  • 4\. Presence of cardiac pacemaker of implanted cardiac defibrillator
  • 5\. Any metal in the head or eyes
  • 6\. Use of medication which decreases seizure threshold
  • 7\. A diagnosis other than stroke is suspected (e.g. brain tumour)
  • 8\. Any severe concomitant chronic medical condition that compromises cardiac or respiratory status,
  • 9\. Significant structural abnormalities of the mouth or throat
  • 10\. Patients requiring oxygen treatment will be excluded at point of entry to prevent further compromise to already impaired respiratory system

Outcomes

Primary Outcomes

Not specified

Similar Trials